Canonical Allele Identifier: CA405300544

Gene: HAMP

Linked Data

• MyVariant Identifiers: chr19:g.35775705C>A (hg19) ; chr19:g.35284802C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284802C>A , CM000681.2:g.35284802C>A	GRCh38
NC_000019.9:g.35775705C>A , CM000681.1:g.35775705C>A	GRCh37
NC_000019.8:g.40467545C>A	NCBI36
NG_011563.1:g.7296C>A
NG_011563.2:g.7296C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.104C>A MANE Select	ENSP00000222304.2:p.Ala35Glu
ENST00000222304.3:c.104C>A	ENSP00000222304.2:p.Ala35Glu
ENST00000593580.1:n.2286C>A
ENST00000598398.5:c.104C>A	ENSP00000471894.1:p.Ala35Glu
NM_021175.2:c.104C>A	NP_066998.1:p.Ala35Glu
NM_021175.3:c.104C>A	NP_066998.1:p.Ala35Glu
NM_021175.4:c.104C>A MANE Select	NP_066998.1:p.Ala35Glu