Canonical Allele Identifier: CA2196373756

Gene: CHD2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.92978257A= , CM000677.2:g.92978257A=	GRCh38
NC_000015.9:g.93521487A= , CM000677.1:g.93521487A=	GRCh37
NC_000015.8:g.91322491A=	NCBI36
NG_012826.1:g.82937A=
NG_012826.2:g.82937A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000625662.3:c.2108A=
ENST00000628118.2:c.1635A=
ENST00000700551.1:c.*1432A=	ENSP00000515057.1:n.*1432A=
ENST00000394196.9:c.2601A= MANE Select	ENSP00000377747.4:p.Thr867=
ENST00000635856.1:n.3173A=
ENST00000636306.1:n.161A=
ENST00000636881.1:c.1972A=
ENST00000637572.1:n.3345A=
ENST00000394196.8:c.2601A=	ENSP00000377747.4:p.Thr867=
ENST00000625463.1:c.141A=	ENSP00000486391.1:p.Thr47=
ENST00000626874.2:c.2601A=	ENSP00000486629.1:p.Thr867=
ENST00000628118.1:n.380A=
NM_001271.3:c.2601A=	NP_001262.3:p.Thr867=
NM_001271.4:c.2601A= MANE Select	NP_001262.3:p.Thr867=