Canonical Allele Identifier: CA392377304

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534768C>G (hg19) ; chr15:g.50242571C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242571C>G , CM000677.2:g.50242571C>G	GRCh38
NC_000015.9:g.50534768C>G , CM000677.1:g.50534768C>G	GRCh37
NC_000015.8:g.48322060C>G	NCBI36
NG_027487.1:g.28395G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1678G>C MANE Select	ENSP00000267845.3:p.Ala560Pro
ENST00000267845.7:c.1678G>C	ENSP00000267845.3:p.Ala560Pro
ENST00000543581.5:c.1579G>C	ENSP00000440252.1:p.Ala527Pro
ENST00000559816.1:n.1422G>C
NM_001306146.1:c.1579G>C	NP_001293075.1:p.Ala527Pro
NM_002112.3:c.1678G>C	NP_002103.2:p.Ala560Pro
XM_011521479.1:c.1441G>C	XP_011519781.1:p.Ala481Pro
XM_011521480.1:c.1246G>C	XP_011519782.1:p.Ala416Pro
XM_017022094.1:c.1783G>C	XP_016877583.1:p.Ala595Pro
XM_017022095.1:c.1684G>C	XP_016877584.1:p.Ala562Pro
XM_017022096.1:c.1555G>C	XP_016877585.1:p.Ala519Pro
XM_017022097.1:c.1546G>C	XP_016877586.1:p.Ala516Pro
XM_017022098.1:c.1351G>C	XP_016877587.1:p.Ala451Pro
NM_002112.4:c.1678G>C MANE Select	NP_002103.2:p.Ala560Pro
NM_001306146.2:c.1579G>C	NP_001293075.1:p.Ala527Pro