Canonical Allele Identifier: CA338621427

Gene: EPHA2

Linked Data

• MyVariant Identifiers: chr1:g.16458560C>G (hg19) ; chr1:g.16132065C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132065C>G , CM000663.2:g.16132065C>G	GRCh38
NC_000001.10:g.16458560C>G , CM000663.1:g.16458560C>G	GRCh37
NC_000001.9:g.16331147C>G	NCBI36
NG_021396.1:g.29023G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2324G>C MANE Select	ENSP00000351209.5:p.Ser775Thr
ENST00000358432.7:c.2324G>C	ENSP00000351209.5:p.Ser775Thr
NM_004431.3:c.2324G>C	NP_004422.2:p.Ser775Thr
NM_001329090.1:c.2162G>C	NP_001316019.1:p.Ser721Thr
NM_004431.4:c.2324G>C	NP_004422.2:p.Ser775Thr
NM_004431.5:c.2324G>C MANE Select	NP_004422.2:p.Ser775Thr
NM_001329090.2:c.2162G>C	NP_001316019.1:p.Ser721Thr