Canonical Allele Identifier: CA2196373759

Gene: CHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978280A= , CM000677.2:g.92978280A=	GRCh38
NC_000015.9:g.93521510A= , CM000677.1:g.93521510A=	GRCh37
NC_000015.8:g.91322514A=	NCBI36
NG_012826.1:g.82960A=
NG_012826.2:g.82960A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000625662.3:c.2131A=
ENST00000628118.2:c.1658A=
ENST00000700551.1:c.*1455A=	ENSP00000515057.1:n.*1455A=
ENST00000394196.9:c.2624A= MANE Select	ENSP00000377747.4:p.Asn875=
ENST00000635856.1:n.3196A=
ENST00000636306.1:n.184A=
ENST00000636881.1:c.1995A=
ENST00000637572.1:n.3368A=
ENST00000394196.8:c.2624A=	ENSP00000377747.4:p.Asn875=
ENST00000625463.1:c.164A=	ENSP00000486391.1:p.Asn55=
ENST00000626874.2:c.2624A=	ENSP00000486629.1:p.Asn875=
ENST00000628118.1:n.403A=
NM_001271.3:c.2624A=	NP_001262.3:p.Asn875=
NM_001271.4:c.2624A= MANE Select	NP_001262.3:p.Asn875=