Canonical Allele Identifier: CA392377004

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534626C>T (hg19) ; chr15:g.50242429C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242429C>T , CM000677.2:g.50242429C>T	GRCh38
NC_000015.9:g.50534626C>T , CM000677.1:g.50534626C>T	GRCh37
NC_000015.8:g.48321918C>T	NCBI36
NG_027487.1:g.28537G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1820G>A MANE Select	ENSP00000267845.3:p.Gly607Glu
ENST00000267845.7:c.1820G>A	ENSP00000267845.3:p.Gly607Glu
ENST00000543581.5:c.1721G>A	ENSP00000440252.1:p.Gly574Glu
ENST00000559816.1:n.1564G>A
NM_001306146.1:c.1721G>A	NP_001293075.1:p.Gly574Glu
NM_002112.3:c.1820G>A	NP_002103.2:p.Gly607Glu
XM_011521479.1:c.1583G>A	XP_011519781.1:p.Gly528Glu
XM_011521480.1:c.1388G>A	XP_011519782.1:p.Gly463Glu
XM_017022094.1:c.1925G>A	XP_016877583.1:p.Gly642Glu
XM_017022095.1:c.1826G>A	XP_016877584.1:p.Gly609Glu
XM_017022096.1:c.1697G>A	XP_016877585.1:p.Gly566Glu
XM_017022097.1:c.1688G>A	XP_016877586.1:p.Gly563Glu
XM_017022098.1:c.1493G>A	XP_016877587.1:p.Gly498Glu
NM_002112.4:c.1820G>A MANE Select	NP_002103.2:p.Gly607Glu
NM_001306146.2:c.1721G>A	NP_001293075.1:p.Gly574Glu