Canonical Allele Identifier: CA416385562
Gene: EPHA2 HGNC NCBI

Linked Data

gnomAD v4: 1-16132151-G-C
MyVariant Identifiers: chr1:g.16458646G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.16132151G>C , CM000663.2:g.16132151G>C GRCh38
NC_000001.10:g.16458646G>C , CM000663.1:g.16458646G>C GRCh37
NC_000001.9:g.16331233G>C NCBI36
NG_021396.1:g.28937C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000358432.8:c.2238C>G MANE Select ENSP00000351209.5:p.Leu746=
ENST00000358432.7:c.2238C>G ENSP00000351209.5:p.Leu746=
NM_004431.3:c.2238C>G NP_004422.2:p.Leu746=
NM_001329090.1:c.2076C>G NP_001316019.1:p.Leu692=
NM_004431.4:c.2238C>G NP_004422.2:p.Leu746=
NM_004431.5:c.2238C>G MANE Select NP_004422.2:p.Leu746=
NM_001329090.2:c.2076C>G NP_001316019.1:p.Leu692=
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