Canonical Allele Identifier: CA392377309

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534770T>C (hg19) ; chr15:g.50242573T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242573T>C , CM000677.2:g.50242573T>C	GRCh38
NC_000015.9:g.50534770T>C , CM000677.1:g.50534770T>C	GRCh37
NC_000015.8:g.48322062T>C	NCBI36
NG_027487.1:g.28393A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1676A>G MANE Select	ENSP00000267845.3:p.Asp559Gly
ENST00000267845.7:c.1676A>G	ENSP00000267845.3:p.Asp559Gly
ENST00000543581.5:c.1577A>G	ENSP00000440252.1:p.Asp526Gly
ENST00000559816.1:n.1420A>G
NM_001306146.1:c.1577A>G	NP_001293075.1:p.Asp526Gly
NM_002112.3:c.1676A>G	NP_002103.2:p.Asp559Gly
XM_011521479.1:c.1439A>G	XP_011519781.1:p.Asp480Gly
XM_011521480.1:c.1244A>G	XP_011519782.1:p.Asp415Gly
XM_017022094.1:c.1781A>G	XP_016877583.1:p.Asp594Gly
XM_017022095.1:c.1682A>G	XP_016877584.1:p.Asp561Gly
XM_017022096.1:c.1553A>G	XP_016877585.1:p.Asp518Gly
XM_017022097.1:c.1544A>G	XP_016877586.1:p.Asp515Gly
XM_017022098.1:c.1349A>G	XP_016877587.1:p.Asp450Gly
NM_002112.4:c.1676A>G MANE Select	NP_002103.2:p.Asp559Gly
NM_001306146.2:c.1577A>G	NP_001293075.1:p.Asp526Gly