Canonical Allele Identifier: CA392377199

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534719T>G (hg19) ; chr15:g.50242522T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242522T>G , CM000677.2:g.50242522T>G	GRCh38
NC_000015.9:g.50534719T>G , CM000677.1:g.50534719T>G	GRCh37
NC_000015.8:g.48322011T>G	NCBI36
NG_027487.1:g.28444A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1727A>C MANE Select	ENSP00000267845.3:p.Gln576Pro
ENST00000267845.7:c.1727A>C	ENSP00000267845.3:p.Gln576Pro
ENST00000543581.5:c.1628A>C	ENSP00000440252.1:p.Gln543Pro
ENST00000559816.1:n.1471A>C
NM_001306146.1:c.1628A>C	NP_001293075.1:p.Gln543Pro
NM_002112.3:c.1727A>C	NP_002103.2:p.Gln576Pro
XM_011521479.1:c.1490A>C	XP_011519781.1:p.Gln497Pro
XM_011521480.1:c.1295A>C	XP_011519782.1:p.Gln432Pro
XM_017022094.1:c.1832A>C	XP_016877583.1:p.Gln611Pro
XM_017022095.1:c.1733A>C	XP_016877584.1:p.Gln578Pro
XM_017022096.1:c.1604A>C	XP_016877585.1:p.Gln535Pro
XM_017022097.1:c.1595A>C	XP_016877586.1:p.Gln532Pro
XM_017022098.1:c.1400A>C	XP_016877587.1:p.Gln467Pro
NM_002112.4:c.1727A>C MANE Select	NP_002103.2:p.Gln576Pro
NM_001306146.2:c.1628A>C	NP_001293075.1:p.Gln543Pro