Canonical Allele Identifier: CA1155649883
Gene: EPHA2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132032C= , CM000663.2:g.16132032C= GRCh38
NC_000001.10:g.16458527C= , CM000663.1:g.16458527C= GRCh37
NC_000001.9:g.16331114C= NCBI36
NG_021396.1:g.29056G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000358432.8:c.2325+32G= MANE Select ENSP00000351209.5:n.2325+32G=
ENST00000358432.7:c.2325+32G= ENSP00000351209.5:n.2325+32G=
NM_004431.3:c.2325+32G= NP_004422.2:n.2325+32G=
NM_001329090.1:c.2163+32G= NP_001316019.1:n.2163+32G=
NM_004431.4:c.2325+32G= NP_004422.2:n.2325+32G=
NM_004431.5:c.2325+32G= MANE Select NP_004422.2:n.2325+32G=
NM_001329090.2:c.2163+32G= NP_001316019.1:n.2163+32G=
Search 100 bp 5'
Search 100 bp 3'