Canonical Allele Identifier: CA338622336

Gene: EPHA2

Linked Data

• dbSNP Id: rs746899152
• MyVariant Identifiers: chr1:g.16458617G>C (hg19) ; chr1:g.16132122G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132122G>C , CM000663.2:g.16132122G>C	GRCh38
NC_000001.10:g.16458617G>C , CM000663.1:g.16458617G>C	GRCh37
NC_000001.9:g.16331204G>C	NCBI36
NG_021396.1:g.28966C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2267C>G MANE Select	ENSP00000351209.5:p.Ser756Cys
ENST00000358432.7:c.2267C>G	ENSP00000351209.5:p.Ser756Cys
NM_004431.3:c.2267C>G	NP_004422.2:p.Ser756Cys
NM_001329090.1:c.2105C>G	NP_001316019.1:p.Ser702Cys
NM_004431.4:c.2267C>G	NP_004422.2:p.Ser756Cys
NM_004431.5:c.2267C>G MANE Select	NP_004422.2:p.Ser756Cys
NM_001329090.2:c.2105C>G	NP_001316019.1:p.Ser702Cys