Canonical Allele Identifier: CA1155650080

Gene: EPHA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132153G= , CM000663.2:g.16132153G=	GRCh38
NC_000001.10:g.16458648G= , CM000663.1:g.16458648G=	GRCh37
NC_000001.9:g.16331235G=	NCBI36
NG_021396.1:g.28935C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2236C= MANE Select	ENSP00000351209.5:p.Leu746=
ENST00000358432.7:c.2236C=	ENSP00000351209.5:p.Leu746=
NM_004431.3:c.2236C=	NP_004422.2:p.Leu746=
NM_001329090.1:c.2074C=	NP_001316019.1:p.Leu692=
NM_004431.4:c.2236C=	NP_004422.2:p.Leu746=
NM_004431.5:c.2236C= MANE Select	NP_004422.2:p.Leu746=
NM_001329090.2:c.2074C=	NP_001316019.1:p.Leu692=