Canonical Allele Identifier: CA392376988

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534618A>T (hg19) ; chr15:g.50242421A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242421A>T , CM000677.2:g.50242421A>T	GRCh38
NC_000015.9:g.50534618A>T , CM000677.1:g.50534618A>T	GRCh37
NC_000015.8:g.48321910A>T	NCBI36
NG_027487.1:g.28545T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1828T>A MANE Select	ENSP00000267845.3:p.Ser610Thr
ENST00000267845.7:c.1828T>A	ENSP00000267845.3:p.Ser610Thr
ENST00000543581.5:c.1729T>A	ENSP00000440252.1:p.Ser577Thr
ENST00000559816.1:n.1572T>A
NM_001306146.1:c.1729T>A	NP_001293075.1:p.Ser577Thr
NM_002112.3:c.1828T>A	NP_002103.2:p.Ser610Thr
XM_011521479.1:c.1591T>A	XP_011519781.1:p.Ser531Thr
XM_011521480.1:c.1396T>A	XP_011519782.1:p.Ser466Thr
XM_017022094.1:c.1933T>A	XP_016877583.1:p.Ser645Thr
XM_017022095.1:c.1834T>A	XP_016877584.1:p.Ser612Thr
XM_017022096.1:c.1705T>A	XP_016877585.1:p.Ser569Thr
XM_017022097.1:c.1696T>A	XP_016877586.1:p.Ser566Thr
XM_017022098.1:c.1501T>A	XP_016877587.1:p.Ser501Thr
NM_002112.4:c.1828T>A MANE Select	NP_002103.2:p.Ser610Thr
NM_001306146.2:c.1729T>A	NP_001293075.1:p.Ser577Thr