Canonical Allele Identifier: CA1202488577

Gene: CD244

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.160838011A= , CM000663.2:g.160838011A=	GRCh38
NC_000001.10:g.160807801A= , CM000663.1:g.160807801A=	GRCh37
NC_000001.9:g.159074425A=	NCBI36
NG_015991.1:g.29892T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368034.9:c.834+440T= MANE Select	ENSP00000357013.4:n.834+440T=
ENST00000322302.7:c.558+440T=	ENSP00000313619.7:n.558+440T=
ENST00000368033.7:c.849+440T=	ENSP00000357012.3:n.849+440T=
ENST00000368034.8:c.834+440T=	ENSP00000357013.4:n.834+440T=
ENST00000481677.1:n.414+440T=
ENST00000492063.5:c.834+440T=	ENSP00000432636.1:n.834+440T=
NM_001166663.1:c.849+440T=	NP_001160135.1:n.849+440T=
NM_001166664.1:c.558+440T=	NP_001160136.1:n.558+440T=
NM_016382.3:c.834+440T=	NP_057466.1:n.834+440T=
XM_011509620.1:c.849+440T=	XP_011507922.1:n.849+440T=
XM_011509621.1:c.849+440T=	XP_011507923.1:n.849+440T=
XM_011509622.1:c.834+440T=	XP_011507924.1:n.834+440T=
XM_011509623.1:c.240+440T=	XP_011507925.1:n.240+440T=
XM_011509621.2:c.849+440T=	XP_011507923.1:n.849+440T=
XM_011509622.2:c.834+440T=	XP_011507924.1:n.834+440T=
XM_011509623.3:c.240+440T=	XP_011507925.1:n.240+440T=
XR_001737229.1:n.1178+440T=
NM_016382.4:c.834+440T= MANE Select	NP_057466.1:n.834+440T=
NM_001166663.2:c.849+440T=	NP_001160135.1:n.849+440T=
NM_001166664.2:c.558+440T=	NP_001160136.1:n.558+440T=