Canonical Allele Identifier: CA392377230

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534733A>C (hg19) ; chr15:g.50242536A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242536A>C , CM000677.2:g.50242536A>C	GRCh38
NC_000015.9:g.50534733A>C , CM000677.1:g.50534733A>C	GRCh37
NC_000015.8:g.48322025A>C	NCBI36
NG_027487.1:g.28430T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1713T>G MANE Select	ENSP00000267845.3:p.Ser571Arg
ENST00000267845.7:c.1713T>G	ENSP00000267845.3:p.Ser571Arg
ENST00000543581.5:c.1614T>G	ENSP00000440252.1:p.Ser538Arg
ENST00000559816.1:n.1457T>G
NM_001306146.1:c.1614T>G	NP_001293075.1:p.Ser538Arg
NM_002112.3:c.1713T>G	NP_002103.2:p.Ser571Arg
XM_011521479.1:c.1476T>G	XP_011519781.1:p.Ser492Arg
XM_011521480.1:c.1281T>G	XP_011519782.1:p.Ser427Arg
XM_017022094.1:c.1818T>G	XP_016877583.1:p.Ser606Arg
XM_017022095.1:c.1719T>G	XP_016877584.1:p.Ser573Arg
XM_017022096.1:c.1590T>G	XP_016877585.1:p.Ser530Arg
XM_017022097.1:c.1581T>G	XP_016877586.1:p.Ser527Arg
XM_017022098.1:c.1386T>G	XP_016877587.1:p.Ser462Arg
NM_002112.4:c.1713T>G MANE Select	NP_002103.2:p.Ser571Arg
NM_001306146.2:c.1614T>G	NP_001293075.1:p.Ser538Arg