Canonical Allele Identifier: CA392377303

Gene: HDC

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1678G>T MANE Select	ENSP00000267845.3:p.Ala560Ser
ENST00000267845.7:c.1678G>T	ENSP00000267845.3:p.Ala560Ser
ENST00000543581.5:c.1579G>T	ENSP00000440252.1:p.Ala527Ser
ENST00000559816.1:n.1422G>T
NM_001306146.1:c.1579G>T	NP_001293075.1:p.Ala527Ser
NM_002112.3:c.1678G>T	NP_002103.2:p.Ala560Ser
XM_011521479.1:c.1441G>T	XP_011519781.1:p.Ala481Ser
XM_011521480.1:c.1246G>T	XP_011519782.1:p.Ala416Ser
XM_017022094.1:c.1783G>T	XP_016877583.1:p.Ala595Ser
XM_017022095.1:c.1684G>T	XP_016877584.1:p.Ala562Ser
XM_017022096.1:c.1555G>T	XP_016877585.1:p.Ala519Ser
XM_017022097.1:c.1546G>T	XP_016877586.1:p.Ala516Ser
XM_017022098.1:c.1351G>T	XP_016877587.1:p.Ala451Ser
NM_002112.4:c.1678G>T MANE Select	NP_002103.2:p.Ala560Ser
NM_001306146.2:c.1579G>T	NP_001293075.1:p.Ala527Ser