Canonical Allele Identifier: CA338622396
Gene: EPHA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132149A>C , CM000663.2:g.16132149A>C GRCh38
NC_000001.10:g.16458644A>C , CM000663.1:g.16458644A>C GRCh37
NC_000001.9:g.16331231A>C NCBI36
NG_021396.1:g.28939T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358432.8:c.2240T>G MANE Select ENSP00000351209.5:p.Val747Gly
ENST00000358432.7:c.2240T>G ENSP00000351209.5:p.Val747Gly
NM_004431.3:c.2240T>G NP_004422.2:p.Val747Gly
NM_001329090.1:c.2078T>G NP_001316019.1:p.Val693Gly
NM_004431.4:c.2240T>G NP_004422.2:p.Val747Gly
NM_004431.5:c.2240T>G MANE Select NP_004422.2:p.Val747Gly
NM_001329090.2:c.2078T>G NP_001316019.1:p.Val693Gly