Canonical Allele Identifier: CA1155650009

Gene: EPHA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132105G= , CM000663.2:g.16132105G=	GRCh38
NC_000001.10:g.16458600G= , CM000663.1:g.16458600G=	GRCh37
NC_000001.9:g.16331187G=	NCBI36
NG_021396.1:g.28983C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2284C= MANE Select	ENSP00000351209.5:p.Arg762=
ENST00000358432.7:c.2284C=	ENSP00000351209.5:p.Arg762=
NM_004431.3:c.2284C=	NP_004422.2:p.Arg762=
NM_001329090.1:c.2122C=	NP_001316019.1:p.Arg708=
NM_004431.4:c.2284C=	NP_004422.2:p.Arg762=
NM_004431.5:c.2284C= MANE Select	NP_004422.2:p.Arg762=
NM_001329090.2:c.2122C=	NP_001316019.1:p.Arg708=