Canonical Allele Identifier: CA9375819
Gene: HAMP HGNC NCBI

Linked Data

dbSNP Id: rs759793237

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284926del , CM000681.2:g.35284926del GRCh38
NC_000019.9:g.35775829del , CM000681.1:g.35775829del GRCh37
NC_000019.8:g.40467669del NCBI36
NG_011563.1:g.7420del
NG_011563.2:g.7420del

Transcript Alleles

HGVS Amino-acid change
ENST00000222304.5:c.151-12del MANE Select ENSP00000222304.2:n.151-12del
ENST00000222304.3:c.151-12del ENSP00000222304.2:n.151-12del
ENST00000593580.1:n.2410del
ENST00000598398.5:c.151-12del ENSP00000471894.1:n.151-12del
NM_021175.2:c.151-12del NP_066998.1:n.151-12del
NM_021175.3:c.151-12del NP_066998.1:n.151-12del
NM_021175.4:c.151-12del MANE Select NP_066998.1:n.151-12del