Canonical Allele Identifier: CA890136093

Gene: EPHA2

Linked Data

• dbSNP Id: rs1271306998
• MyVariant Identifiers: chr1:g.16458528T>A (hg19) ; chr1:g.16132033T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.16132033T>A , CM000663.2:g.16132033T>A	GRCh38
NC_000001.10:g.16458528T>A , CM000663.1:g.16458528T>A	GRCh37
NC_000001.9:g.16331115T>A	NCBI36
NG_021396.1:g.29055A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358432.8:c.2325+31A>T MANE Select	ENSP00000351209.5:n.2325+31A>T
ENST00000358432.7:c.2325+31A>T	ENSP00000351209.5:n.2325+31A>T
NM_004431.3:c.2325+31A>T	NP_004422.2:n.2325+31A>T
NM_001329090.1:c.2163+31A>T	NP_001316019.1:n.2163+31A>T
NM_004431.4:c.2325+31A>T	NP_004422.2:n.2325+31A>T
NM_004431.5:c.2325+31A>T MANE Select	NP_004422.2:n.2325+31A>T
NM_001329090.2:c.2163+31A>T	NP_001316019.1:n.2163+31A>T