Canonical Allele Identifier: CA392377079

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534662T>C (hg19) ; chr15:g.50242465T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242465T>C , CM000677.2:g.50242465T>C	GRCh38
NC_000015.9:g.50534662T>C , CM000677.1:g.50534662T>C	GRCh37
NC_000015.8:g.48321954T>C	NCBI36
NG_027487.1:g.28501A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1784A>G MANE Select	ENSP00000267845.3:p.Gln595Arg
ENST00000267845.7:c.1784A>G	ENSP00000267845.3:p.Gln595Arg
ENST00000543581.5:c.1685A>G	ENSP00000440252.1:p.Gln562Arg
ENST00000559816.1:n.1528A>G
NM_001306146.1:c.1685A>G	NP_001293075.1:p.Gln562Arg
NM_002112.3:c.1784A>G	NP_002103.2:p.Gln595Arg
XM_011521479.1:c.1547A>G	XP_011519781.1:p.Gln516Arg
XM_011521480.1:c.1352A>G	XP_011519782.1:p.Gln451Arg
XM_017022094.1:c.1889A>G	XP_016877583.1:p.Gln630Arg
XM_017022095.1:c.1790A>G	XP_016877584.1:p.Gln597Arg
XM_017022096.1:c.1661A>G	XP_016877585.1:p.Gln554Arg
XM_017022097.1:c.1652A>G	XP_016877586.1:p.Gln551Arg
XM_017022098.1:c.1457A>G	XP_016877587.1:p.Gln486Arg
NM_002112.4:c.1784A>G MANE Select	NP_002103.2:p.Gln595Arg
NM_001306146.2:c.1685A>G	NP_001293075.1:p.Gln562Arg