Canonical Allele Identifier: CA1139845571

Gene: DISC1 TSNAX-DISC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.232040449G= , CM000663.2:g.232040449G=	GRCh38
NC_000001.10:g.232176195G= , CM000663.1:g.232176195G=	GRCh37
NC_000001.9:g.230242818G=	NCBI36
NG_011681.1:g.418635G=
NG_011681.2:g.418635G=

Transcript Alleles

HGVS	Amino-acid Change
NM_018662.3:c.*3618G= (DISC1) MANE Select	NP_061132.2:n.*3618G=
ENST00000439617.8:c.*3618G= (DISC1) MANE Select	ENSP00000403888.4:n.*3618G=
NM_001012957.1:c.*3618G= (DISC1)	NP_001012975.1:n.*3618G=
NM_001012957.2:c.*3618G= (DISC1)	NP_001012975.1:n.*3618G=
NM_001164537.1:c.*3618G= (DISC1)	NP_001158009.1:n.*3618G=
NM_001164537.2:c.*3618G= (DISC1)	NP_001158009.1:n.*3618G=
NM_001164540.1:c.*3618G= (DISC1)	NP_001158012.1:n.*3618G=
NM_001164540.2:c.*3618G= (DISC1)	NP_001158012.1:n.*3618G=
NM_018662.2:c.*3618G= (DISC1)	NP_061132.2:n.*3618G=
NR_028393.1:n.6849G= (TSNAX-DISC1)
ENST00000366637.7:c.*3618G= (DISC1)	ENSP00000355597.5:n.*3618G=
ENST00000366637.8:c.*3618G= (DISC1)	ENSP00000355597.6:n.*3618G=
ENST00000439617.6:c.*3618G= (DISC1)	ENSP00000403888.2:n.*3618G=
ENST00000620189.3:c.*3618G= (DISC1)	ENSP00000482174.1:n.*3618G=
ENST00000622252.4:c.*4724G= (DISC1)	ENSP00000481791.1:n.*4724G=