Canonical Allele Identifier: CA338621435

Gene: EPHA2

Linked Data

• MyVariant Identifiers: chr1:g.16458561T>C (hg19) ; chr1:g.16132066T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132066T>C , CM000663.2:g.16132066T>C	GRCh38
NC_000001.10:g.16458561T>C , CM000663.1:g.16458561T>C	GRCh37
NC_000001.9:g.16331148T>C	NCBI36
NG_021396.1:g.29022A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2323A>G MANE Select	ENSP00000351209.5:p.Ser775Gly
ENST00000358432.7:c.2323A>G	ENSP00000351209.5:p.Ser775Gly
NM_004431.3:c.2323A>G	NP_004422.2:p.Ser775Gly
NM_001329090.1:c.2161A>G	NP_001316019.1:p.Ser721Gly
NM_004431.4:c.2323A>G	NP_004422.2:p.Ser775Gly
NM_004431.5:c.2323A>G MANE Select	NP_004422.2:p.Ser775Gly
NM_001329090.2:c.2161A>G	NP_001316019.1:p.Ser721Gly