Canonical Allele Identifier: CA338622335

Gene: EPHA2

Linked Data

• gnomAD v4: 1-16132122-G-A
• MyVariant Identifiers: chr1:g.16458617G>A (hg19) ; chr1:g.16132122G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2267C>T MANE Select	ENSP00000351209.5:p.Ser756Phe
ENST00000358432.7:c.2267C>T	ENSP00000351209.5:p.Ser756Phe
NM_004431.3:c.2267C>T	NP_004422.2:p.Ser756Phe
NM_001329090.1:c.2105C>T	NP_001316019.1:p.Ser702Phe
NM_004431.4:c.2267C>T	NP_004422.2:p.Ser756Phe
NM_004431.5:c.2267C>T MANE Select	NP_004422.2:p.Ser756Phe
NM_001329090.2:c.2105C>T	NP_001316019.1:p.Ser702Phe