Canonical Allele Identifier: CA392377076

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534661C>A (hg19) ; chr15:g.50242464C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242464C>A , CM000677.2:g.50242464C>A	GRCh38
NC_000015.9:g.50534661C>A , CM000677.1:g.50534661C>A	GRCh37
NC_000015.8:g.48321953C>A	NCBI36
NG_027487.1:g.28502G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1785G>T MANE Select	ENSP00000267845.3:p.Gln595His
ENST00000267845.7:c.1785G>T	ENSP00000267845.3:p.Gln595His
ENST00000543581.5:c.1686G>T	ENSP00000440252.1:p.Gln562His
ENST00000559816.1:n.1529G>T
NM_001306146.1:c.1686G>T	NP_001293075.1:p.Gln562His
NM_002112.3:c.1785G>T	NP_002103.2:p.Gln595His
XM_011521479.1:c.1548G>T	XP_011519781.1:p.Gln516His
XM_011521480.1:c.1353G>T	XP_011519782.1:p.Gln451His
XM_017022094.1:c.1890G>T	XP_016877583.1:p.Gln630His
XM_017022095.1:c.1791G>T	XP_016877584.1:p.Gln597His
XM_017022096.1:c.1662G>T	XP_016877585.1:p.Gln554His
XM_017022097.1:c.1653G>T	XP_016877586.1:p.Gln551His
XM_017022098.1:c.1458G>T	XP_016877587.1:p.Gln486His
NM_002112.4:c.1785G>T MANE Select	NP_002103.2:p.Gln595His
NM_001306146.2:c.1686G>T	NP_001293075.1:p.Gln562His