Canonical Allele Identifier: CA1227118060
Gene: DISC1 HGNC NCBI
TSNAX-DISC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.231812900G>T , CM000663.2:g.231812900G>T GRCh38
NC_000001.10:g.231948646G>T , CM000663.1:g.231948646G>T GRCh37
NC_000001.9:g.230015269G>T NCBI36
NG_011681.1:g.191086G>T
NG_011681.2:g.191086G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000366637.8:c.1793-5429G>T (DISC1) ENSP00000355597.6:n.1793-5429G>T
ENST00000439617.8:c.1793-5429G>T (DISC1) MANE Select ENSP00000403888.4:n.1793-5429G>T
ENST00000644515.1:c.*1939-5429G>T (TSNAX-DISC1) ENSP00000496433.1:n.*1939-5429G>T
ENST00000646525.1:c.*1884-5429G>T (TSNAX-DISC1) ENSP00000494923.1:n.*1884-5429G>T
ENST00000295051.11:c.*94-5429G>T (DISC1) ENSP00000295051.7:n.*94-5429G>T
ENST00000366632.6:c.*493-5429G>T (DISC1) ENSP00000355592.2:n.*493-5429G>T
ENST00000366633.7:c.1793-5429G>T (DISC1) ENSP00000355593.3:n.1793-5429G>T
ENST00000366636.8:c.1793-5429G>T (DISC1) ENSP00000355596.4:n.1793-5429G>T
ENST00000366637.7:c.1793-5429G>T (DISC1) ENSP00000355597.5:n.1793-5429G>T
ENST00000422590.6:c.*1654-5429G>T (DISC1) ENSP00000415147.2:n.*1654-5429G>T
ENST00000439617.6:c.1793-5429G>T (DISC1) ENSP00000403888.2:n.1793-5429G>T
ENST00000535944.5:c.*142-5429G>T (DISC1) ENSP00000441193.1:n.*142-5429G>T
ENST00000535983.5:c.1793-5429G>T (DISC1) ENSP00000443996.1:n.1793-5429G>T
ENST00000537876.5:c.1793-330G>T (DISC1) ENSP00000440909.2:n.1793-330G>T
ENST00000539444.5:c.1690-5429G>T (DISC1) ENSP00000440953.1:n.1690-5429G>T
ENST00000602281.5:c.1793-5429G>T (DISC1) ENSP00000473425.1:n.1793-5429G>T
ENST00000602567.1:c.*1820-5429G>T (TSNAX-DISC1) ENSP00000473456.1:n.*1820-5429G>T
ENST00000602634.5:c.*1939-5429G>T (TSNAX-DISC1) ENSP00000473307.1:n.*1939-5429G>T
ENST00000602700.5:c.*494-5429G>T (DISC1) ENSP00000473417.1:n.*494-5429G>T
ENST00000602713.5:c.*652-5429G>T (DISC1) ENSP00000473261.1:n.*652-5429G>T
ENST00000602822.5:c.*652-5429G>T (DISC1) ENSP00000473586.1:n.*652-5429G>T
ENST00000602873.5:c.585-5429G>T (DISC1) ENSP00000473386.1:n.585-5429G>T
ENST00000602885.5:c.*1852-5429G>T (TSNAX-DISC1) ENSP00000473476.1:n.*1852-5429G>T
ENST00000602956.5:c.*1654-5429G>T (TSNAX-DISC1) ENSP00000473532.1:n.*1654-5429G>T
ENST00000602962.5:c.*1923-5429G>T (TSNAX-DISC1) ENSP00000473367.1:n.*1923-5429G>T
ENST00000620189.3:c.1427-5429G>T (DISC1) ENSP00000482174.1:n.1427-5429G>T
ENST00000622252.4:c.*334-5429G>T (DISC1) ENSP00000481791.1:n.*334-5429G>T
ENST00000628350.2:c.1634+41830G>T (DISC1) ENSP00000487190.1:n.1634+41830G>T
NM_001012957.1:c.1793-5429G>T (DISC1) NP_001012975.1:n.1793-5429G>T
NM_001012959.1:c.1793-5429G>T (DISC1) NP_001012977.1:n.1793-5429G>T
NM_001164537.1:c.1889-5429G>T (DISC1) NP_001158009.1:n.1889-5429G>T
NM_001164538.1:c.1793-5429G>T (DISC1) NP_001158010.1:n.1793-5429G>T
NM_001164539.1:c.1793-5429G>T (DISC1) NP_001158011.1:n.1793-5429G>T
NM_001164540.1:c.1427-5429G>T (DISC1) NP_001158012.1:n.1427-5429G>T
NM_001164541.1:c.1793-5429G>T (DISC1) NP_001158013.1:n.1793-5429G>T
NM_001164542.1:c.1793-5429G>T (DISC1) NP_001158014.1:n.1793-5429G>T
NM_001164544.1:c.1793-5429G>T (DISC1) NP_001158016.1:n.1793-5429G>T
NM_001164545.1:c.1690-5429G>T (DISC1) NP_001158017.1:n.1690-5429G>T
NM_001164546.1:c.1634+41830G>T (DISC1) NP_001158018.1:n.1634+41830G>T
NM_001164547.1:c.1634+41830G>T (DISC1) NP_001158019.1:n.1634+41830G>T
NM_001164548.1:c.1635-5429G>T (DISC1) NP_001158020.1:n.1635-5429G>T
NM_001164556.1:c.585-5429G>T (DISC1) NP_001158028.1:n.585-5429G>T
NM_018662.2:c.1793-5429G>T (DISC1) NP_061132.2:n.1793-5429G>T
NR_028393.1:n.2459-5429G>T (TSNAX-DISC1)
NR_028394.1:n.2642-5429G>T (TSNAX-DISC1)
NR_028395.1:n.2539-5429G>T (TSNAX-DISC1)
NR_028396.1:n.2514-5429G>T (TSNAX-DISC1)
NR_028397.1:n.2379-5429G>T (TSNAX-DISC1)
NR_028398.1:n.2133-5429G>T (TSNAX-DISC1)
XR_949268.1:n.2771C>A
XR_949269.1:n.2448C>A
XR_949270.1:n.1434C>A
XR_001738521.2:n.1476C>A
XR_949268.3:n.1716C>A
XR_949269.2:n.1606C>A
XR_949270.2:n.1432C>A
NM_001012957.2:c.1793-5429G>T (DISC1) NP_001012975.1:n.1793-5429G>T
NM_001012959.2:c.1793-5429G>T (DISC1) NP_001012977.1:n.1793-5429G>T
NM_001164537.2:c.1889-5429G>T (DISC1) NP_001158009.1:n.1889-5429G>T
NM_001164538.2:c.1793-5429G>T (DISC1) NP_001158010.1:n.1793-5429G>T
NM_001164539.2:c.1793-5429G>T (DISC1) NP_001158011.1:n.1793-5429G>T
NM_001164540.2:c.1427-5429G>T (DISC1) NP_001158012.1:n.1427-5429G>T
NM_001164541.2:c.1793-5429G>T (DISC1) NP_001158013.1:n.1793-5429G>T
NM_001164542.2:c.1793-5429G>T (DISC1) NP_001158014.1:n.1793-5429G>T
NM_001164546.2:c.1634+41830G>T (DISC1) NP_001158018.1:n.1634+41830G>T
NM_001164547.2:c.1634+41830G>T (DISC1) NP_001158019.1:n.1634+41830G>T
NM_018662.3:c.1793-5429G>T (DISC1) MANE Select NP_061132.2:n.1793-5429G>T
NM_001164544.2:c.1793-5429G>T (DISC1) NP_001158016.1:n.1793-5429G>T
NM_001164545.2:c.1690-5429G>T (DISC1) NP_001158017.1:n.1690-5429G>T
NM_001164548.2:c.1635-5429G>T (DISC1) NP_001158020.1:n.1635-5429G>T
NM_001164556.2:c.585-5429G>T (DISC1) NP_001158028.1:n.585-5429G>T