Canonical Allele Identifier: CA2333586120

Gene: HAMP

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.35284981T= , CM000681.2:g.35284981T=	GRCh38
NC_000019.9:g.35775884T= , CM000681.1:g.35775884T=	GRCh37
NC_000019.8:g.40467724T=	NCBI36
NG_011563.1:g.7475T=
NG_011563.2:g.7475T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222304.5:c.194T= MANE Select	ENSP00000222304.2:p.Ile65=
ENST00000222304.3:c.194T=	ENSP00000222304.2:p.Ile65=
ENST00000593580.1:n.2465T=
ENST00000598398.5:c.194T=	ENSP00000471894.1:p.Ile65=
NM_021175.2:c.194T=	NP_066998.1:p.Ile65=
NM_021175.3:c.194T=	NP_066998.1:p.Ile65=
NM_021175.4:c.194T= MANE Select	NP_066998.1:p.Ile65=