Canonical Allele Identifier: CA392376940

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534594A>T (hg19) ; chr15:g.50242397A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242397A>T , CM000677.2:g.50242397A>T	GRCh38
NC_000015.9:g.50534594A>T , CM000677.1:g.50534594A>T	GRCh37
NC_000015.8:g.48321886A>T	NCBI36
NG_027487.1:g.28569T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1852T>A MANE Select	ENSP00000267845.3:p.Phe618Ile
ENST00000267845.7:c.1852T>A	ENSP00000267845.3:p.Phe618Ile
ENST00000543581.5:c.1753T>A	ENSP00000440252.1:p.Phe585Ile
ENST00000559816.1:n.1596T>A
NM_001306146.1:c.1753T>A	NP_001293075.1:p.Phe585Ile
NM_002112.3:c.1852T>A	NP_002103.2:p.Phe618Ile
XM_011521479.1:c.1615T>A	XP_011519781.1:p.Phe539Ile
XM_011521480.1:c.1420T>A	XP_011519782.1:p.Phe474Ile
XM_017022094.1:c.1957T>A	XP_016877583.1:p.Phe653Ile
XM_017022095.1:c.1858T>A	XP_016877584.1:p.Phe620Ile
XM_017022096.1:c.1729T>A	XP_016877585.1:p.Phe577Ile
XM_017022097.1:c.1720T>A	XP_016877586.1:p.Phe574Ile
XM_017022098.1:c.1525T>A	XP_016877587.1:p.Phe509Ile
NM_002112.4:c.1852T>A MANE Select	NP_002103.2:p.Phe618Ile
NM_001306146.2:c.1753T>A	NP_001293075.1:p.Phe585Ile