Canonical Allele Identifier: CA1566570162

Gene: CHD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.98881073T= , CM000667.2:g.98881073T=	GRCh38
NC_000005.9:g.98216777T= , CM000667.1:g.98216777T=	GRCh37
NC_000005.8:g.98244677T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000511067.3:c.3060+3A=	ENSP00000479403.2:n.3060+3A=
ENST00000706140.1:n.3207+3A=
ENST00000706141.1:c.*588+3A=	ENSP00000516225.1:n.*588+3A=
ENST00000614616.5:c.3060+3A= MANE Select	ENSP00000483667.1:n.3060+3A=
ENST00000284049.7:c.3060+3A=	ENSP00000284049.3:n.3060+3A=
ENST00000614616.4:c.3060+3A=	ENSP00000483667.1:n.3060+3A=
NM_001270.2:c.3060+3A=	NP_001261.2:n.3060+3A=
XM_005271866.3:c.3060+3A=	XP_005271923.1:n.3060+3A=
XM_005271867.3:c.3060+3A=	XP_005271924.1:n.3060+3A=
XM_011543112.1:c.3060+3A=	XP_011541414.1:n.3060+3A=
XR_427702.2:n.3292+3A=
XR_948231.1:n.3293+3A=
NM_001364113.1:c.3060+3A=	NP_001351042.1:n.3060+3A=
NR_157078.1:n.4414+3A=
NR_157079.1:n.4384+3A=
XM_005271867.5:c.3060+3A=	XP_005271924.1:n.3060+3A=
XM_017008991.1:c.273+3A=	XP_016864480.1:n.273+3A=
XM_017008992.1:c.273+3A=	XP_016864481.1:n.273+3A=
XM_024454344.1:c.3060+3A=	XP_024310112.1:n.3060+3A=
XM_024454345.1:c.3060+3A=	XP_024310113.1:n.3060+3A=
XR_001741986.2:n.4442+3A=
XR_002959841.1:n.4442+3A=
NM_001270.4:c.3060+3A= MANE Select	NP_001261.2:n.3060+3A=
NM_001364113.3:c.3060+3A=	NP_001351042.1:n.3060+3A=
NM_001376194.2:c.3060+3A=	NP_001363123.1:n.3060+3A=
NR_157078.3:n.3707+3A=
NR_157079.3:n.3677+3A=