Canonical Allele Identifier: CA405300526

Gene: HAMP

Linked Data

• MyVariant Identifiers: chr19:g.35775704G>A (hg19) ; chr19:g.35284801G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284801G>A , CM000681.2:g.35284801G>A	GRCh38
NC_000019.9:g.35775704G>A , CM000681.1:g.35775704G>A	GRCh37
NC_000019.8:g.40467544G>A	NCBI36
NG_011563.1:g.7295G>A
NG_011563.2:g.7295G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.103G>A MANE Select	ENSP00000222304.2:p.Ala35Thr
ENST00000222304.3:c.103G>A	ENSP00000222304.2:p.Ala35Thr
ENST00000593580.1:n.2285G>A
ENST00000598398.5:c.103G>A	ENSP00000471894.1:p.Ala35Thr
NM_021175.2:c.103G>A	NP_066998.1:p.Ala35Thr
NM_021175.3:c.103G>A	NP_066998.1:p.Ala35Thr
NM_021175.4:c.103G>A MANE Select	NP_066998.1:p.Ala35Thr