Canonical Allele Identifier: CA2068077934

Gene: HPD

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121846911C= , CM000674.2:g.121846911C=	GRCh38
NC_000012.11:g.122284817C= , CM000674.1:g.122284817C=	GRCh37
NC_000012.10:g.120769200C=	NCBI36
NG_016461.1:g.46701G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289004.8:c.782G= MANE Select	ENSP00000289004.4:p.Gly261=
ENST00000543163.5:c.665G=	ENSP00000441677.1:p.Gly222=
NM_001171993.1:c.665G=	NP_001165464.1:p.Gly222=
NM_002150.2:c.782G=	NP_002141.1:p.Gly261=
NM_002150.3:c.782G= MANE Select	NP_002141.2:p.Gly261=
NM_001171993.2:c.665G=	NP_001165464.1:p.Gly222=