Canonical Allele Identifier: CA2651020209
Gene: DISC1 HGNC NCBI
TSNAX-DISC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.232037094A>G , CM000663.2:g.232037094A>G GRCh38
NC_000001.10:g.232172840A>G , CM000663.1:g.232172840A>G GRCh37
NC_000001.9:g.230239463A>G NCBI36
NG_011681.1:g.415280A>G
NG_011681.2:g.415280A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000366637.8:c.*263A>G (DISC1) ENSP00000355597.6:n.*263A>G
ENST00000439617.8:c.*263A>G (DISC1) MANE Select ENSP00000403888.4:n.*263A>G
ENST00000366637.7:c.*263A>G (DISC1) ENSP00000355597.5:n.*263A>G
ENST00000439617.6:c.*263A>G (DISC1) ENSP00000403888.2:n.*263A>G
ENST00000620189.3:c.*263A>G (DISC1) ENSP00000482174.1:n.*263A>G
ENST00000622252.4:c.*1369A>G (DISC1) ENSP00000481791.1:n.*1369A>G
NM_001012957.1:c.*263A>G (DISC1) NP_001012975.1:n.*263A>G
NM_001164537.1:c.*263A>G (DISC1) NP_001158009.1:n.*263A>G
NM_001164540.1:c.*263A>G (DISC1) NP_001158012.1:n.*263A>G
NM_018662.2:c.*263A>G (DISC1) NP_061132.2:n.*263A>G
NR_028393.1:n.3494A>G (TSNAX-DISC1)
NM_001012957.2:c.*263A>G (DISC1) NP_001012975.1:n.*263A>G
NM_001164537.2:c.*263A>G (DISC1) NP_001158009.1:n.*263A>G
NM_001164540.2:c.*263A>G (DISC1) NP_001158012.1:n.*263A>G
NM_018662.3:c.*263A>G (DISC1) MANE Select NP_061132.2:n.*263A>G