Canonical Allele Identifier: CA416385486

Gene: EPHA2

Linked Data

• gnomAD v4: 1-16132103-G-T
• MyVariant Identifiers: chr1:g.16458598G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132103G>T , CM000663.2:g.16132103G>T	GRCh38
NC_000001.10:g.16458598G>T , CM000663.1:g.16458598G>T	GRCh37
NC_000001.9:g.16331185G>T	NCBI36
NG_021396.1:g.28985C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2286C>A MANE Select	ENSP00000351209.5:p.Arg762=
ENST00000358432.7:c.2286C>A	ENSP00000351209.5:p.Arg762=
NM_004431.3:c.2286C>A	NP_004422.2:p.Arg762=
NM_001329090.1:c.2124C>A	NP_001316019.1:p.Arg708=
NM_004431.4:c.2286C>A	NP_004422.2:p.Arg762=
NM_004431.5:c.2286C>A MANE Select	NP_004422.2:p.Arg762=
NM_001329090.2:c.2124C>A	NP_001316019.1:p.Arg708=