Canonical Allele Identifier: CA1155649991

Gene: EPHA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132093C= , CM000663.2:g.16132093C=	GRCh38
NC_000001.10:g.16458588C= , CM000663.1:g.16458588C=	GRCh37
NC_000001.9:g.16331175C=	NCBI36
NG_021396.1:g.28995G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2296G= MANE Select	ENSP00000351209.5:p.Asp766=
ENST00000358432.7:c.2296G=	ENSP00000351209.5:p.Asp766=
NM_004431.3:c.2296G=	NP_004422.2:p.Asp766=
NM_001329090.1:c.2134G=	NP_001316019.1:p.Asp712=
NM_004431.4:c.2296G=	NP_004422.2:p.Asp766=
NM_004431.5:c.2296G= MANE Select	NP_004422.2:p.Asp766=
NM_001329090.2:c.2134G=	NP_001316019.1:p.Asp712=