Canonical Allele Identifier: CA338622395
Gene: EPHA2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.16458644A>T (hg19) chr1:g.16132149A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132149A>T , CM000663.2:g.16132149A>T GRCh38
NC_000001.10:g.16458644A>T , CM000663.1:g.16458644A>T GRCh37
NC_000001.9:g.16331231A>T NCBI36
NG_021396.1:g.28939T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000358432.8:c.2240T>A MANE Select ENSP00000351209.5:p.Val747Asp
ENST00000358432.7:c.2240T>A ENSP00000351209.5:p.Val747Asp
NM_004431.3:c.2240T>A NP_004422.2:p.Val747Asp
NM_001329090.1:c.2078T>A NP_001316019.1:p.Val693Asp
NM_004431.4:c.2240T>A NP_004422.2:p.Val747Asp
NM_004431.5:c.2240T>A MANE Select NP_004422.2:p.Val747Asp
NM_001329090.2:c.2078T>A NP_001316019.1:p.Val693Asp
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