Canonical Allele Identifier: CA416226486

Gene: EPHA2

Linked Data

• MyVariant Identifiers: chr1:g.16458559A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132064A>G , CM000663.2:g.16132064A>G	GRCh38
NC_000001.10:g.16458559A>G , CM000663.1:g.16458559A>G	GRCh37
NC_000001.9:g.16331146A>G	NCBI36
NG_021396.1:g.29024T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2325T>C MANE Select	ENSP00000351209.5:p.Ser775=
ENST00000358432.7:c.2325T>C	ENSP00000351209.5:p.Ser775=
NM_004431.3:c.2325T>C	NP_004422.2:p.Ser775=
NM_001329090.1:c.2163T>C	NP_001316019.1:p.Ser721=
NM_004431.4:c.2325T>C	NP_004422.2:p.Ser775=
NM_004431.5:c.2325T>C MANE Select	NP_004422.2:p.Ser775=
NM_001329090.2:c.2163T>C	NP_001316019.1:p.Ser721=