Canonical Allele Identifier: CA490314272

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534766G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242569G>C , CM000677.2:g.50242569G>C	GRCh38
NC_000015.9:g.50534766G>C , CM000677.1:g.50534766G>C	GRCh37
NC_000015.8:g.48322058G>C	NCBI36
NG_027487.1:g.28397C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1680C>G MANE Select	ENSP00000267845.3:p.Ala560=
ENST00000267845.7:c.1680C>G	ENSP00000267845.3:p.Ala560=
ENST00000543581.5:c.1581C>G	ENSP00000440252.1:p.Ala527=
ENST00000559816.1:n.1424C>G
NM_001306146.1:c.1581C>G	NP_001293075.1:p.Ala527=
NM_002112.3:c.1680C>G	NP_002103.2:p.Ala560=
XM_011521479.1:c.1443C>G	XP_011519781.1:p.Ala481=
XM_011521480.1:c.1248C>G	XP_011519782.1:p.Ala416=
XM_017022094.1:c.1785C>G	XP_016877583.1:p.Ala595=
XM_017022095.1:c.1686C>G	XP_016877584.1:p.Ala562=
XM_017022096.1:c.1557C>G	XP_016877585.1:p.Ala519=
XM_017022097.1:c.1548C>G	XP_016877586.1:p.Ala516=
XM_017022098.1:c.1353C>G	XP_016877587.1:p.Ala451=
NM_002112.4:c.1680C>G MANE Select	NP_002103.2:p.Ala560=
NM_001306146.2:c.1581C>G	NP_001293075.1:p.Ala527=