Canonical Allele Identifier: CA338622345

Gene: EPHA2

Linked Data

• dbSNP Id: rs2024581511
• gnomAD v4: 1-16132126-C-T
• MyVariant Identifiers: chr1:g.16458621C>T (hg19) ; chr1:g.16132126C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132126C>T , CM000663.2:g.16132126C>T	GRCh38
NC_000001.10:g.16458621C>T , CM000663.1:g.16458621C>T	GRCh37
NC_000001.9:g.16331208C>T	NCBI36
NG_021396.1:g.28962G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2263G>A MANE Select	ENSP00000351209.5:p.Val755Met
ENST00000358432.7:c.2263G>A	ENSP00000351209.5:p.Val755Met
NM_004431.3:c.2263G>A	NP_004422.2:p.Val755Met
NM_001329090.1:c.2101G>A	NP_001316019.1:p.Val701Met
NM_004431.4:c.2263G>A	NP_004422.2:p.Val755Met
NM_004431.5:c.2263G>A MANE Select	NP_004422.2:p.Val755Met
NM_001329090.2:c.2101G>A	NP_001316019.1:p.Val701Met