Canonical Allele Identifier: CA2333586044

Gene: HAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284863G= , CM000681.2:g.35284863G=	GRCh38
NC_000019.9:g.35775766G= , CM000681.1:g.35775766G=	GRCh37
NC_000019.8:g.40467606G=	NCBI36
NG_011563.1:g.7357G=
NG_011563.2:g.7357G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.150+15G= MANE Select	ENSP00000222304.2:n.150+15G=
ENST00000222304.3:c.150+15G=	ENSP00000222304.2:n.150+15G=
ENST00000593580.1:n.2347G=
ENST00000598398.5:c.150+15G=	ENSP00000471894.1:n.150+15G=
NM_021175.2:c.150+15G=	NP_066998.1:n.150+15G=
NM_021175.3:c.150+15G=	NP_066998.1:n.150+15G=
NM_021175.4:c.150+15G= MANE Select	NP_066998.1:n.150+15G=