Canonical Allele Identifier: CA1394098690

Gene: CD200R1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.112962738A= , CM000665.2:g.112962738A=	GRCh38
NC_000003.11:g.112681585A= , CM000665.1:g.112681585A=	GRCh37
NC_000003.10:g.114164275A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308611.8:c.67+12053T= MANE Select	ENSP00000311035.3:n.67+12053T=
ENST00000295863.4:c.67+12053T=	ENSP00000295863.4:n.67+12053T=
ENST00000308611.7:c.67+12053T=	ENSP00000311035.3:n.67+12053T=
ENST00000440122.6:c.67+12053T=	ENSP00000405733.2:n.67+12053T=
ENST00000471858.5:c.67+12053T=	ENSP00000418928.1:n.67+12053T=
ENST00000490004.1:c.67+12053T=	ENSP00000418801.1:n.67+12053T=
NM_138806.3:c.67+12053T=	NP_620161.1:n.67+12053T=
NM_138939.2:c.67+12053T=	NP_620385.1:n.67+12053T=
NM_138940.2:c.67+12053T=	NP_620386.1:n.67+12053T=
NM_170780.2:c.67+12053T=	NP_740750.1:n.67+12053T=
XM_006713492.2:c.67+12053T=	XP_006713555.1:n.67+12053T=
NM_138806.4:c.67+12053T= MANE Select	NP_620161.1:n.67+12053T=
NM_138939.3:c.67+12053T=	NP_620385.1:n.67+12053T=
NM_138940.3:c.67+12053T=	NP_620386.1:n.67+12053T=
NM_170780.3:c.67+12053T=	NP_740750.1:n.67+12053T=