Canonical Allele Identifier: CA405300842
Gene: HAMP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284837G>C , CM000681.2:g.35284837G>C GRCh38
NC_000019.9:g.35775740G>C , CM000681.1:g.35775740G>C GRCh37
NC_000019.8:g.40467580G>C NCBI36
NG_011563.1:g.7331G>C
NG_011563.2:g.7331G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.139G>C MANE Select ENSP00000222304.2:p.Ala47Pro
ENST00000222304.3:c.139G>C ENSP00000222304.2:p.Ala47Pro
ENST00000593580.1:n.2321G>C
ENST00000598398.5:c.139G>C ENSP00000471894.1:p.Ala47Pro
NM_021175.2:c.139G>C NP_066998.1:p.Ala47Pro
NM_021175.3:c.139G>C NP_066998.1:p.Ala47Pro
NM_021175.4:c.139G>C MANE Select NP_066998.1:p.Ala47Pro