Canonical Allele Identifier: CA338642093
Gene: EPHA2 HGNC NCBI

Linked Data

dbSNP Id: rs113882203

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16148725C>A , CM000663.2:g.16148725C>A GRCh38
NC_000001.10:g.16475220C>A , CM000663.1:g.16475220C>A GRCh37
NC_000001.9:g.16347807C>A NCBI36
NG_021396.1:g.12363G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000358432.8:c.476G>T MANE Select ENSP00000351209.5:p.Arg159Leu
ENST00000358432.7:c.476G>T ENSP00000351209.5:p.Arg159Leu
ENST00000461614.1:n.528G>T
NM_004431.3:c.476G>T NP_004422.2:p.Arg159Leu
NM_001329090.1:c.314G>T NP_001316019.1:p.Arg105Leu
NM_004431.4:c.476G>T NP_004422.2:p.Arg159Leu
XM_017000537.1:c.476G>T XP_016856026.1:p.Arg159Leu
NM_004431.5:c.476G>T MANE Select NP_004422.2:p.Arg159Leu
NM_001329090.2:c.314G>T NP_001316019.1:p.Arg105Leu