Canonical Allele Identifier: CA1155650061

Gene: EPHA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132143C= , CM000663.2:g.16132143C=	GRCh38
NC_000001.10:g.16458638C= , CM000663.1:g.16458638C=	GRCh37
NC_000001.9:g.16331225C=	NCBI36
NG_021396.1:g.28945G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2246G= MANE Select	ENSP00000351209.5:p.Ser749=
ENST00000358432.7:c.2246G=	ENSP00000351209.5:p.Ser749=
NM_004431.3:c.2246G=	NP_004422.2:p.Ser749=
NM_001329090.1:c.2084G=	NP_001316019.1:p.Ser695=
NM_004431.4:c.2246G=	NP_004422.2:p.Ser749=
NM_004431.5:c.2246G= MANE Select	NP_004422.2:p.Ser749=
NM_001329090.2:c.2084G=	NP_001316019.1:p.Ser695=