Canonical Allele Identifier: CA2333586022

Gene: HAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284815C= , CM000681.2:g.35284815C=	GRCh38
NC_000019.9:g.35775718C= , CM000681.1:g.35775718C=	GRCh37
NC_000019.8:g.40467558C=	NCBI36
NG_011563.1:g.7309C=
NG_011563.2:g.7309C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222304.5:c.117C= MANE Select	ENSP00000222304.2:p.Pro39=
ENST00000222304.3:c.117C=	ENSP00000222304.2:p.Pro39=
ENST00000593580.1:n.2299C=
ENST00000598398.5:c.117C=	ENSP00000471894.1:p.Pro39=
NM_021175.2:c.117C=	NP_066998.1:p.Pro39=
NM_021175.3:c.117C=	NP_066998.1:p.Pro39=
NM_021175.4:c.117C= MANE Select	NP_066998.1:p.Pro39=