Canonical Allele Identifier: CA732775472
Gene: DISC1 HGNC NCBI
TSNAX-DISC1 HGNC NCBI

Linked Data

dbSNP Id: rs843979

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.231994862C>T , CM000663.2:g.231994862C>T GRCh38
NC_000001.10:g.232130608C>T , CM000663.1:g.232130608C>T GRCh37
NC_000001.9:g.230197231C>T NCBI36
NG_011681.1:g.373048C>T
NG_011681.2:g.373048C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000366637.8:c.2043-13923C>T (DISC1) ENSP00000355597.6:n.2043-13923C>T
ENST00000439617.8:c.2043-13923C>T (DISC1) MANE Select ENSP00000403888.4:n.2043-13923C>T
ENST00000366637.7:c.2043-13923C>T (DISC1) ENSP00000355597.5:n.2043-13923C>T
ENST00000422590.6:c.*1904-13923C>T (DISC1) ENSP00000415147.2:n.*1904-13923C>T
ENST00000427560.1:n.308-13923C>T (DISC1)
ENST00000439617.6:c.2043-13923C>T (DISC1) ENSP00000403888.2:n.2043-13923C>T
ENST00000535983.5:c.1982-13923C>T (DISC1) ENSP00000443996.1:n.1982-13923C>T
ENST00000620189.3:c.1677-13923C>T (DISC1) ENSP00000482174.1:n.1677-13923C>T
ENST00000622252.4:c.*584-13923C>T (DISC1) ENSP00000481791.1:n.*584-13923C>T
NM_001012957.1:c.2043-13923C>T (DISC1) NP_001012975.1:n.2043-13923C>T
NM_001164537.1:c.2139-13923C>T (DISC1) NP_001158009.1:n.2139-13923C>T
NM_001164538.1:c.2043-13923C>T (DISC1) NP_001158010.1:n.2043-13923C>T
NM_001164540.1:c.1677-13923C>T (DISC1) NP_001158012.1:n.1677-13923C>T
NM_001164541.1:c.1982-13923C>T (DISC1) NP_001158013.1:n.1982-13923C>T
NM_001164547.1:c.*16-13923C>T (DISC1) NP_001158019.1:n.*16-13923C>T
NM_018662.2:c.2043-13923C>T (DISC1) NP_061132.2:n.2043-13923C>T
NR_028393.1:n.2709-13923C>T (TSNAX-DISC1)
NM_001012957.2:c.2043-13923C>T (DISC1) NP_001012975.1:n.2043-13923C>T
NM_001164537.2:c.2139-13923C>T (DISC1) NP_001158009.1:n.2139-13923C>T
NM_001164538.2:c.2043-13923C>T (DISC1) NP_001158010.1:n.2043-13923C>T
NM_001164540.2:c.1677-13923C>T (DISC1) NP_001158012.1:n.1677-13923C>T
NM_001164541.2:c.1982-13923C>T (DISC1) NP_001158013.1:n.1982-13923C>T
NM_001164547.2:c.*16-13923C>T (DISC1) NP_001158019.1:n.*16-13923C>T
NM_018662.3:c.2043-13923C>T (DISC1) MANE Select NP_061132.2:n.2043-13923C>T