Canonical Allele Identifier: CA1142063002
Gene: EPHA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132150C= , CM000663.2:g.16132150C= GRCh38
NC_000001.10:g.16458645C= , CM000663.1:g.16458645C= GRCh37
NC_000001.9:g.16331232C= NCBI36
NG_021396.1:g.28938G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358432.8:c.2239G= MANE Select ENSP00000351209.5:p.Val747=
ENST00000358432.7:c.2239G= ENSP00000351209.5:p.Val747=
NM_004431.3:c.2239G= NP_004422.2:p.Val747=
NM_001329090.1:c.2077G= NP_001316019.1:p.Val693=
NM_004431.4:c.2239G= NP_004422.2:p.Val747=
NM_004431.5:c.2239G= MANE Select NP_004422.2:p.Val747=
NM_001329090.2:c.2077G= NP_001316019.1:p.Val693=