Canonical Allele Identifier: CA392377104

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534674G>C (hg19) ; chr15:g.50242477G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242477G>C , CM000677.2:g.50242477G>C	GRCh38
NC_000015.9:g.50534674G>C , CM000677.1:g.50534674G>C	GRCh37
NC_000015.8:g.48321966G>C	NCBI36
NG_027487.1:g.28489C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1772C>G MANE Select	ENSP00000267845.3:p.Pro591Arg
ENST00000267845.7:c.1772C>G	ENSP00000267845.3:p.Pro591Arg
ENST00000543581.5:c.1673C>G	ENSP00000440252.1:p.Pro558Arg
ENST00000559816.1:n.1516C>G
NM_001306146.1:c.1673C>G	NP_001293075.1:p.Pro558Arg
NM_002112.3:c.1772C>G	NP_002103.2:p.Pro591Arg
XM_011521479.1:c.1535C>G	XP_011519781.1:p.Pro512Arg
XM_011521480.1:c.1340C>G	XP_011519782.1:p.Pro447Arg
XM_017022094.1:c.1877C>G	XP_016877583.1:p.Pro626Arg
XM_017022095.1:c.1778C>G	XP_016877584.1:p.Pro593Arg
XM_017022096.1:c.1649C>G	XP_016877585.1:p.Pro550Arg
XM_017022097.1:c.1640C>G	XP_016877586.1:p.Pro547Arg
XM_017022098.1:c.1445C>G	XP_016877587.1:p.Pro482Arg
NM_002112.4:c.1772C>G MANE Select	NP_002103.2:p.Pro591Arg
NM_001306146.2:c.1673C>G	NP_001293075.1:p.Pro558Arg