Canonical Allele Identifier: CA1594027288

Gene: HAVCR2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157104725C= , CM000667.2:g.157104725C=	GRCh38
NC_000005.9:g.156531736C= , CM000667.1:g.156531736C=	GRCh37
NC_000005.8:g.156464314C=	NCBI36
NG_030444.1:g.9513G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032782.5:c.419G= MANE Select	NP_116171.3:p.Arg140=
ENST00000307851.9:c.419G= MANE Select	ENSP00000312002.4:p.Arg140=
NM_032782.4:c.419G=	NP_116171.3:p.Arg140=
ENST00000307851.8:c.419G=	ENSP00000312002.4:p.Arg140=
ENST00000517358.3:c.68G=	ENSP00000513313.1:p.Arg23=
ENST00000521665.1:n.682G=
ENST00000521665.2:c.68G=	ENSP00000513314.1:p.Arg23=
ENST00000522593.5:c.394+1902G=	ENSP00000430873.1:n.394+1902G=
ENST00000522593.6:c.394+1902G=	ENSP00000430873.1:n.394+1902G=
ENST00000524219.1:c.68G=	ENSP00000430328.1:p.Arg23=
ENST00000524219.2:c.68G=	ENSP00000430328.2:p.Arg23=
ENST00000696897.1:c.419G=	ENSP00000512959.1:p.Arg140=
ENST00000696899.1:c.419G=	ENSP00000512960.1:p.Arg140=
ENST00000696900.1:c.68G=	ENSP00000512961.1:p.Arg23=
ENST00000696901.1:c.394+1902G=	ENSP00000512962.1:n.394+1902G=
ENST00000696902.1:c.419G=	ENSP00000512963.1:p.Arg140=