Canonical Allele Identifier: CA405300791
Gene: HAMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284832C>G , CM000681.2:g.35284832C>G GRCh38
NC_000019.9:g.35775735C>G , CM000681.1:g.35775735C>G GRCh37
NC_000019.8:g.40467575C>G NCBI36
NG_011563.1:g.7326C>G
NG_011563.2:g.7326C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.134C>G MANE Select ENSP00000222304.2:p.Ala45Gly
ENST00000222304.3:c.134C>G ENSP00000222304.2:p.Ala45Gly
ENST00000593580.1:n.2316C>G
ENST00000598398.5:c.134C>G ENSP00000471894.1:p.Ala45Gly
NM_021175.2:c.134C>G NP_066998.1:p.Ala45Gly
NM_021175.3:c.134C>G NP_066998.1:p.Ala45Gly
NM_021175.4:c.134C>G MANE Select NP_066998.1:p.Ala45Gly