Canonical Allele Identifier: CA392377078

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534662T>G (hg19) ; chr15:g.50242465T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242465T>G , CM000677.2:g.50242465T>G	GRCh38
NC_000015.9:g.50534662T>G , CM000677.1:g.50534662T>G	GRCh37
NC_000015.8:g.48321954T>G	NCBI36
NG_027487.1:g.28501A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1784A>C MANE Select	ENSP00000267845.3:p.Gln595Pro
ENST00000267845.7:c.1784A>C	ENSP00000267845.3:p.Gln595Pro
ENST00000543581.5:c.1685A>C	ENSP00000440252.1:p.Gln562Pro
ENST00000559816.1:n.1528A>C
NM_001306146.1:c.1685A>C	NP_001293075.1:p.Gln562Pro
NM_002112.3:c.1784A>C	NP_002103.2:p.Gln595Pro
XM_011521479.1:c.1547A>C	XP_011519781.1:p.Gln516Pro
XM_011521480.1:c.1352A>C	XP_011519782.1:p.Gln451Pro
XM_017022094.1:c.1889A>C	XP_016877583.1:p.Gln630Pro
XM_017022095.1:c.1790A>C	XP_016877584.1:p.Gln597Pro
XM_017022096.1:c.1661A>C	XP_016877585.1:p.Gln554Pro
XM_017022097.1:c.1652A>C	XP_016877586.1:p.Gln551Pro
XM_017022098.1:c.1457A>C	XP_016877587.1:p.Gln486Pro
NM_002112.4:c.1784A>C MANE Select	NP_002103.2:p.Gln595Pro
NM_001306146.2:c.1685A>C	NP_001293075.1:p.Gln562Pro