Canonical Allele Identifier: CA2333586137

Gene: HAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35285015A= , CM000681.2:g.35285015A=	GRCh38
NC_000019.9:g.35775918A= , CM000681.1:g.35775918A=	GRCh37
NC_000019.8:g.40467758A=	NCBI36
NG_011563.1:g.7509A=
NG_011563.2:g.7509A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222304.5:c.228A= MANE Select	ENSP00000222304.2:p.Ser76=
ENST00000222304.3:c.228A=	ENSP00000222304.2:p.Ser76=
ENST00000593580.1:n.2499A=
ENST00000598398.5:c.228A=	ENSP00000471894.1:p.Ser76=
NM_021175.2:c.228A=	NP_066998.1:p.Ser76=
NM_021175.3:c.228A=	NP_066998.1:p.Ser76=
NM_021175.4:c.228A= MANE Select	NP_066998.1:p.Ser76=