Canonical Allele Identifier: CA490314155

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534694G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242497G>T , CM000677.2:g.50242497G>T	GRCh38
NC_000015.9:g.50534694G>T , CM000677.1:g.50534694G>T	GRCh37
NC_000015.8:g.48321986G>T	NCBI36
NG_027487.1:g.28469C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1752C>A MANE Select	ENSP00000267845.3:p.Ser584=
ENST00000267845.7:c.1752C>A	ENSP00000267845.3:p.Ser584=
ENST00000543581.5:c.1653C>A	ENSP00000440252.1:p.Ser551=
ENST00000559816.1:n.1496C>A
NM_001306146.1:c.1653C>A	NP_001293075.1:p.Ser551=
NM_002112.3:c.1752C>A	NP_002103.2:p.Ser584=
XM_011521479.1:c.1515C>A	XP_011519781.1:p.Ser505=
XM_011521480.1:c.1320C>A	XP_011519782.1:p.Ser440=
XM_017022094.1:c.1857C>A	XP_016877583.1:p.Ser619=
XM_017022095.1:c.1758C>A	XP_016877584.1:p.Ser586=
XM_017022096.1:c.1629C>A	XP_016877585.1:p.Ser543=
XM_017022097.1:c.1620C>A	XP_016877586.1:p.Ser540=
XM_017022098.1:c.1425C>A	XP_016877587.1:p.Ser475=
NM_002112.4:c.1752C>A MANE Select	NP_002103.2:p.Ser584=
NM_001306146.2:c.1653C>A	NP_001293075.1:p.Ser551=