Canonical Allele Identifier: CA1155650058
Gene: EPHA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132142G= , CM000663.2:g.16132142G= GRCh38
NC_000001.10:g.16458637G= , CM000663.1:g.16458637G= GRCh37
NC_000001.9:g.16331224G= NCBI36
NG_021396.1:g.28946C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358432.8:c.2247C= MANE Select ENSP00000351209.5:p.Ser749=
ENST00000358432.7:c.2247C= ENSP00000351209.5:p.Ser749=
NM_004431.3:c.2247C= NP_004422.2:p.Ser749=
NM_001329090.1:c.2085C= NP_001316019.1:p.Ser695=
NM_004431.4:c.2247C= NP_004422.2:p.Ser749=
NM_004431.5:c.2247C= MANE Select NP_004422.2:p.Ser749=
NM_001329090.2:c.2085C= NP_001316019.1:p.Ser695=