Canonical Allele Identifier: CA2739313116

Gene: DISC1 TSNAX-DISC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.232013187T>A , CM000663.2:g.232013187T>A	GRCh38
NC_000001.10:g.232148933T>A , CM000663.1:g.232148933T>A	GRCh37
NC_000001.9:g.230215556T>A	NCBI36
NG_011681.1:g.391373T>A
NG_011681.2:g.391373T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366637.8:c.2241+4204T>A (DISC1)	ENSP00000355597.6:n.2241+4204T>A
ENST00000439617.8:c.2307+4138T>A (DISC1) MANE Select	ENSP00000403888.4:n.2307+4138T>A
ENST00000366637.7:c.2241+4204T>A (DISC1)	ENSP00000355597.5:n.2241+4204T>A
ENST00000439617.6:c.2307+4138T>A (DISC1)	ENSP00000403888.2:n.2307+4138T>A
ENST00000620189.3:c.1941+4138T>A (DISC1)	ENSP00000482174.1:n.1941+4138T>A
ENST00000622252.4:c.*848+4138T>A (DISC1)	ENSP00000481791.1:n.*848+4138T>A
NM_001012957.1:c.2241+4204T>A (DISC1)	NP_001012975.1:n.2241+4204T>A
NM_001164537.1:c.2403+4138T>A (DISC1)	NP_001158009.1:n.2403+4138T>A
NM_001164540.1:c.1941+4138T>A (DISC1)	NP_001158012.1:n.1941+4138T>A
NM_018662.2:c.2307+4138T>A (DISC1)	NP_061132.2:n.2307+4138T>A
NR_028393.1:n.2973+4138T>A (TSNAX-DISC1)
NM_001012957.2:c.2241+4204T>A (DISC1)	NP_001012975.1:n.2241+4204T>A
NM_001164537.2:c.2403+4138T>A (DISC1)	NP_001158009.1:n.2403+4138T>A
NM_001164540.2:c.1941+4138T>A (DISC1)	NP_001158012.1:n.1941+4138T>A
NM_018662.3:c.2307+4138T>A (DISC1) MANE Select	NP_061132.2:n.2307+4138T>A