Canonical Allele Identifier: CA482193495

Gene: HPD

Linked Data

• MyVariant Identifiers: chr12:g.122285027G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.121847121G>T , CM000674.2:g.121847121G>T	GRCh38
NC_000012.11:g.122285027G>T , CM000674.1:g.122285027G>T	GRCh37
NC_000012.10:g.120769410G>T	NCBI36
NG_016461.1:g.46491C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000289004.8:c.690C>A MANE Select	ENSP00000289004.4:p.Ala230=
ENST00000543163.5:c.573C>A	ENSP00000441677.1:p.Ala191=
NM_001171993.1:c.573C>A	NP_001165464.1:p.Ala191=
NM_002150.2:c.690C>A	NP_002141.1:p.Ala230=
NM_002150.3:c.690C>A MANE Select	NP_002141.2:p.Ala230=
NM_001171993.2:c.573C>A	NP_001165464.1:p.Ala191=