Canonical Allele Identifier: CA2196373724

Gene: CHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978170A= , CM000677.2:g.92978170A=	GRCh38
NC_000015.9:g.93521400A= , CM000677.1:g.93521400A=	GRCh37
NC_000015.8:g.91322404A=	NCBI36
NG_012826.1:g.82850A=
NG_012826.2:g.82850A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625662.3:c.2085-64A=
ENST00000628118.2:c.1548A=
ENST00000700551.1:c.*1409-64A=	ENSP00000515057.1:n.*1409-64A=
ENST00000394196.9:c.2578-64A= MANE Select	ENSP00000377747.4:n.2578-64A=
ENST00000635856.1:n.3150-64A=
ENST00000636306.1:n.138-64A=
ENST00000636881.1:c.1949-64A=
ENST00000637572.1:n.3322-64A=
ENST00000394196.8:c.2578-64A=	ENSP00000377747.4:n.2578-64A=
ENST00000625463.1:c.118-64A=	ENSP00000486391.1:n.118-64A=
ENST00000626874.2:c.2578-64A=	ENSP00000486629.1:n.2578-64A=
ENST00000628118.1:n.293A=
NM_001271.3:c.2578-64A=	NP_001262.3:n.2578-64A=
NM_001271.4:c.2578-64A= MANE Select	NP_001262.3:n.2578-64A=