Canonical Allele Identifier: CA1140095343

Gene: CD244

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160839213G= , CM000663.2:g.160839213G=	GRCh38
NC_000001.10:g.160809003G= , CM000663.1:g.160809003G=	GRCh37
NC_000001.9:g.159075627G=	NCBI36
NG_015991.1:g.28690C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368034.9:c.656-164C= MANE Select	ENSP00000357013.4:n.656-164C=
ENST00000322302.7:c.380-164C=	ENSP00000313619.7:n.380-164C=
ENST00000368033.7:c.671-164C=	ENSP00000357012.3:n.671-164C=
ENST00000368034.8:c.656-164C=	ENSP00000357013.4:n.656-164C=
ENST00000492063.5:c.656-164C=	ENSP00000432636.1:n.656-164C=
NM_001166663.1:c.671-164C=	NP_001160135.1:n.671-164C=
NM_001166664.1:c.380-164C=	NP_001160136.1:n.380-164C=
NM_016382.3:c.656-164C=	NP_057466.1:n.656-164C=
XM_011509620.1:c.671-164C=	XP_011507922.1:n.671-164C=
XM_011509621.1:c.671-164C=	XP_011507923.1:n.671-164C=
XM_011509622.1:c.656-164C=	XP_011507924.1:n.656-164C=
XM_011509623.1:c.62-164C=	XP_011507925.1:n.62-164C=
XM_011509621.2:c.671-164C=	XP_011507923.1:n.671-164C=
XM_011509622.2:c.656-164C=	XP_011507924.1:n.656-164C=
XM_011509623.3:c.62-164C=	XP_011507925.1:n.62-164C=
XR_001737229.1:n.881-164C=
NM_016382.4:c.656-164C= MANE Select	NP_057466.1:n.656-164C=
NM_001166663.2:c.671-164C=	NP_001160135.1:n.671-164C=
NM_001166664.2:c.380-164C=	NP_001160136.1:n.380-164C=