Canonical Allele Identifier: CA392377191

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534716G>C (hg19) ; chr15:g.50242519G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242519G>C , CM000677.2:g.50242519G>C	GRCh38
NC_000015.9:g.50534716G>C , CM000677.1:g.50534716G>C	GRCh37
NC_000015.8:g.48322008G>C	NCBI36
NG_027487.1:g.28447C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1730C>G MANE Select	ENSP00000267845.3:p.Thr577Ser
ENST00000267845.7:c.1730C>G	ENSP00000267845.3:p.Thr577Ser
ENST00000543581.5:c.1631C>G	ENSP00000440252.1:p.Thr544Ser
ENST00000559816.1:n.1474C>G
NM_001306146.1:c.1631C>G	NP_001293075.1:p.Thr544Ser
NM_002112.3:c.1730C>G	NP_002103.2:p.Thr577Ser
XM_011521479.1:c.1493C>G	XP_011519781.1:p.Thr498Ser
XM_011521480.1:c.1298C>G	XP_011519782.1:p.Thr433Ser
XM_017022094.1:c.1835C>G	XP_016877583.1:p.Thr612Ser
XM_017022095.1:c.1736C>G	XP_016877584.1:p.Thr579Ser
XM_017022096.1:c.1607C>G	XP_016877585.1:p.Thr536Ser
XM_017022097.1:c.1598C>G	XP_016877586.1:p.Thr533Ser
XM_017022098.1:c.1403C>G	XP_016877587.1:p.Thr468Ser
NM_002112.4:c.1730C>G MANE Select	NP_002103.2:p.Thr577Ser
NM_001306146.2:c.1631C>G	NP_001293075.1:p.Thr544Ser