Canonical Allele Identifier: CA416226490

Gene: EPHA2

Linked Data

• gnomAD v4: 1-16132067-G-C
• MyVariant Identifiers: chr1:g.16458562G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132067G>C , CM000663.2:g.16132067G>C	GRCh38
NC_000001.10:g.16458562G>C , CM000663.1:g.16458562G>C	GRCh37
NC_000001.9:g.16331149G>C	NCBI36
NG_021396.1:g.29021C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2322C>G MANE Select	ENSP00000351209.5:p.Thr774=
ENST00000358432.7:c.2322C>G	ENSP00000351209.5:p.Thr774=
NM_004431.3:c.2322C>G	NP_004422.2:p.Thr774=
NM_001329090.1:c.2160C>G	NP_001316019.1:p.Thr720=
NM_004431.4:c.2322C>G	NP_004422.2:p.Thr774=
NM_004431.5:c.2322C>G MANE Select	NP_004422.2:p.Thr774=
NM_001329090.2:c.2160C>G	NP_001316019.1:p.Thr720=