Canonical Allele Identifier: CA392376953

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534600A>T (hg19) ; chr15:g.50242403A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242403A>T , CM000677.2:g.50242403A>T	GRCh38
NC_000015.9:g.50534600A>T , CM000677.1:g.50534600A>T	GRCh37
NC_000015.8:g.48321892A>T	NCBI36
NG_027487.1:g.28563T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1846T>A MANE Select	ENSP00000267845.3:p.Ser616Thr
ENST00000267845.7:c.1846T>A	ENSP00000267845.3:p.Ser616Thr
ENST00000543581.5:c.1747T>A	ENSP00000440252.1:p.Ser583Thr
ENST00000559816.1:n.1590T>A
NM_001306146.1:c.1747T>A	NP_001293075.1:p.Ser583Thr
NM_002112.3:c.1846T>A	NP_002103.2:p.Ser616Thr
XM_011521479.1:c.1609T>A	XP_011519781.1:p.Ser537Thr
XM_011521480.1:c.1414T>A	XP_011519782.1:p.Ser472Thr
XM_017022094.1:c.1951T>A	XP_016877583.1:p.Ser651Thr
XM_017022095.1:c.1852T>A	XP_016877584.1:p.Ser618Thr
XM_017022096.1:c.1723T>A	XP_016877585.1:p.Ser575Thr
XM_017022097.1:c.1714T>A	XP_016877586.1:p.Ser572Thr
XM_017022098.1:c.1519T>A	XP_016877587.1:p.Ser507Thr
NM_002112.4:c.1846T>A MANE Select	NP_002103.2:p.Ser616Thr
NM_001306146.2:c.1747T>A	NP_001293075.1:p.Ser583Thr