Canonical Allele Identifier: CA732768697
Gene: DISC1 HGNC NCBI
TSNAX-DISC1 HGNC NCBI

Linked Data

dbSNP Id: rs1427718409

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.231827707G>C , CM000663.2:g.231827707G>C GRCh38
NC_000001.10:g.231963453G>C , CM000663.1:g.231963453G>C GRCh37
NC_000001.9:g.230030076G>C NCBI36
NG_011681.1:g.205893G>C
NG_011681.2:g.205893G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000366637.8:c.1981+9190G>C (DISC1) ENSP00000355597.6:n.1981+9190G>C
ENST00000439617.8:c.1981+9190G>C (DISC1) MANE Select ENSP00000403888.4:n.1981+9190G>C
ENST00000366632.6:c.*681+9190G>C (DISC1) ENSP00000355592.2:n.*681+9190G>C
ENST00000366633.7:c.1981+9190G>C (DISC1) ENSP00000355593.3:n.1981+9190G>C
ENST00000366636.8:c.1981+9190G>C (DISC1) ENSP00000355596.4:n.1981+9190G>C
ENST00000366637.7:c.1981+9190G>C (DISC1) ENSP00000355597.5:n.1981+9190G>C
ENST00000422590.6:c.*1842+9190G>C (DISC1) ENSP00000415147.2:n.*1842+9190G>C
ENST00000427560.1:n.246+8557G>C (DISC1)
ENST00000439617.6:c.1981+9190G>C (DISC1) ENSP00000403888.2:n.1981+9190G>C
ENST00000535983.5:c.1981+9190G>C (DISC1) ENSP00000443996.1:n.1981+9190G>C
ENST00000537876.5:c.*264+9190G>C (DISC1) ENSP00000440909.2:n.*264+9190G>C
ENST00000602713.5:c.*840+9190G>C (DISC1) ENSP00000473261.1:n.*840+9190G>C
ENST00000620189.3:c.1615+9190G>C (DISC1) ENSP00000482174.1:n.1615+9190G>C
ENST00000622252.4:c.*522+9190G>C (DISC1) ENSP00000481791.1:n.*522+9190G>C
ENST00000628350.2:c.1634+56637G>C (DISC1) ENSP00000487190.1:n.1634+56637G>C
NM_001012957.1:c.1981+9190G>C (DISC1) NP_001012975.1:n.1981+9190G>C
NM_001012959.1:c.1981+9190G>C (DISC1) NP_001012977.1:n.1981+9190G>C
NM_001164537.1:c.2077+9190G>C (DISC1) NP_001158009.1:n.2077+9190G>C
NM_001164538.1:c.1981+9190G>C (DISC1) NP_001158010.1:n.1981+9190G>C
NM_001164539.1:c.1981+9190G>C (DISC1) NP_001158011.1:n.1981+9190G>C
NM_001164540.1:c.1615+9190G>C (DISC1) NP_001158012.1:n.1615+9190G>C
NM_001164541.1:c.1981+9190G>C (DISC1) NP_001158013.1:n.1981+9190G>C
NM_001164542.1:c.1981+9190G>C (DISC1) NP_001158014.1:n.1981+9190G>C
NM_001164546.1:c.1634+56637G>C (DISC1) NP_001158018.1:n.1634+56637G>C
NM_001164547.1:c.1634+56637G>C (DISC1) NP_001158019.1:n.1634+56637G>C
NM_018662.2:c.1981+9190G>C (DISC1) NP_061132.2:n.1981+9190G>C
NR_028393.1:n.2647+9190G>C (TSNAX-DISC1)
XR_949268.1:n.1270-4873C>G
XR_949269.1:n.1057-13416C>G
XR_949268.3:n.215-4873C>G
XR_949269.2:n.215-13416C>G
NM_001012957.2:c.1981+9190G>C (DISC1) NP_001012975.1:n.1981+9190G>C
NM_001012959.2:c.1981+9190G>C (DISC1) NP_001012977.1:n.1981+9190G>C
NM_001164537.2:c.2077+9190G>C (DISC1) NP_001158009.1:n.2077+9190G>C
NM_001164538.2:c.1981+9190G>C (DISC1) NP_001158010.1:n.1981+9190G>C
NM_001164539.2:c.1981+9190G>C (DISC1) NP_001158011.1:n.1981+9190G>C
NM_001164540.2:c.1615+9190G>C (DISC1) NP_001158012.1:n.1615+9190G>C
NM_001164541.2:c.1981+9190G>C (DISC1) NP_001158013.1:n.1981+9190G>C
NM_001164542.2:c.1981+9190G>C (DISC1) NP_001158014.1:n.1981+9190G>C
NM_001164546.2:c.1634+56637G>C (DISC1) NP_001158018.1:n.1634+56637G>C
NM_001164547.2:c.1634+56637G>C (DISC1) NP_001158019.1:n.1634+56637G>C
NM_018662.3:c.1981+9190G>C (DISC1) MANE Select NP_061132.2:n.1981+9190G>C