Canonical Allele Identifier: CA392377128

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534685G>C (hg19) ; chr15:g.50242488G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242488G>C , CM000677.2:g.50242488G>C	GRCh38
NC_000015.9:g.50534685G>C , CM000677.1:g.50534685G>C	GRCh37
NC_000015.8:g.48321977G>C	NCBI36
NG_027487.1:g.28478C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1761C>G MANE Select	ENSP00000267845.3:p.Cys587Trp
ENST00000267845.7:c.1761C>G	ENSP00000267845.3:p.Cys587Trp
ENST00000543581.5:c.1662C>G	ENSP00000440252.1:p.Cys554Trp
ENST00000559816.1:n.1505C>G
NM_001306146.1:c.1662C>G	NP_001293075.1:p.Cys554Trp
NM_002112.3:c.1761C>G	NP_002103.2:p.Cys587Trp
XM_011521479.1:c.1524C>G	XP_011519781.1:p.Cys508Trp
XM_011521480.1:c.1329C>G	XP_011519782.1:p.Cys443Trp
XM_017022094.1:c.1866C>G	XP_016877583.1:p.Cys622Trp
XM_017022095.1:c.1767C>G	XP_016877584.1:p.Cys589Trp
XM_017022096.1:c.1638C>G	XP_016877585.1:p.Cys546Trp
XM_017022097.1:c.1629C>G	XP_016877586.1:p.Cys543Trp
XM_017022098.1:c.1434C>G	XP_016877587.1:p.Cys478Trp
NM_002112.4:c.1761C>G MANE Select	NP_002103.2:p.Cys587Trp
NM_001306146.2:c.1662C>G	NP_001293075.1:p.Cys554Trp