Canonical Allele Identifier: CA387012579

Gene: HPD

Linked Data

• MyVariant Identifiers: chr12:g.122284790T>G (hg19) ; chr12:g.121846884T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121846884T>G , CM000674.2:g.121846884T>G	GRCh38
NC_000012.11:g.122284790T>G , CM000674.1:g.122284790T>G	GRCh37
NC_000012.10:g.120769173T>G	NCBI36
NG_016461.1:g.46728A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289004.8:c.809A>C MANE Select	ENSP00000289004.4:p.Lys270Thr
ENST00000543163.5:c.692A>C	ENSP00000441677.1:p.Lys231Thr
NM_001171993.1:c.692A>C	NP_001165464.1:p.Lys231Thr
NM_002150.2:c.809A>C	NP_002141.1:p.Lys270Thr
NM_002150.3:c.809A>C MANE Select	NP_002141.2:p.Lys270Thr
NM_001171993.2:c.692A>C	NP_001165464.1:p.Lys231Thr