Canonical Allele Identifier: CA1227184738

Gene: DISC1 TSNAX-DISC1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.231966518G>T , CM000663.2:g.231966518G>T	GRCh38
NC_000001.10:g.232102264G>T , CM000663.1:g.232102264G>T	GRCh37
NC_000001.9:g.230168887G>T	NCBI36
NG_011681.1:g.344704G>T
NG_011681.2:g.344704G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366637.8:c.2042+7630G>T (DISC1)	ENSP00000355597.6:n.2042+7630G>T
ENST00000439617.8:c.2042+7630G>T (DISC1) MANE Select	ENSP00000403888.4:n.2042+7630G>T
ENST00000366637.7:c.2042+7630G>T (DISC1)	ENSP00000355597.5:n.2042+7630G>T
ENST00000422590.6:c.*1903+7630G>T (DISC1)	ENSP00000415147.2:n.*1903+7630G>T
ENST00000427560.1:n.307+7630G>T (DISC1)
ENST00000439617.6:c.2042+7630G>T (DISC1)	ENSP00000403888.2:n.2042+7630G>T
ENST00000535983.5:c.1982-42267G>T (DISC1)	ENSP00000443996.1:n.1982-42267G>T
ENST00000620189.3:c.1676+7630G>T (DISC1)	ENSP00000482174.1:n.1676+7630G>T
ENST00000622252.4:c.*583+7630G>T (DISC1)	ENSP00000481791.1:n.*583+7630G>T
NM_001012957.1:c.2042+7630G>T (DISC1)	NP_001012975.1:n.2042+7630G>T
NM_001164537.1:c.2138+7630G>T (DISC1)	NP_001158009.1:n.2138+7630G>T
NM_001164538.1:c.2042+7630G>T (DISC1)	NP_001158010.1:n.2042+7630G>T
NM_001164540.1:c.1676+7630G>T (DISC1)	NP_001158012.1:n.1676+7630G>T
NM_001164541.1:c.1982-42267G>T (DISC1)	NP_001158013.1:n.1982-42267G>T
NM_001164547.1:c.*15+7630G>T (DISC1)	NP_001158019.1:n.*15+7630G>T
NM_018662.2:c.2042+7630G>T (DISC1)	NP_061132.2:n.2042+7630G>T
NR_028393.1:n.2708+7630G>T (TSNAX-DISC1)
NM_001012957.2:c.2042+7630G>T (DISC1)	NP_001012975.1:n.2042+7630G>T
NM_001164537.2:c.2138+7630G>T (DISC1)	NP_001158009.1:n.2138+7630G>T
NM_001164538.2:c.2042+7630G>T (DISC1)	NP_001158010.1:n.2042+7630G>T
NM_001164540.2:c.1676+7630G>T (DISC1)	NP_001158012.1:n.1676+7630G>T
NM_001164541.2:c.1982-42267G>T (DISC1)	NP_001158013.1:n.1982-42267G>T
NM_001164547.2:c.*15+7630G>T (DISC1)	NP_001158019.1:n.*15+7630G>T
NM_018662.3:c.2042+7630G>T (DISC1) MANE Select	NP_061132.2:n.2042+7630G>T