Canonical Allele Identifier: CA392377166

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534705T>C (hg19) ; chr15:g.50242508T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242508T>C , CM000677.2:g.50242508T>C	GRCh38
NC_000015.9:g.50534705T>C , CM000677.1:g.50534705T>C	GRCh37
NC_000015.8:g.48321997T>C	NCBI36
NG_027487.1:g.28458A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1741A>G MANE Select	ENSP00000267845.3:p.Thr581Ala
ENST00000267845.7:c.1741A>G	ENSP00000267845.3:p.Thr581Ala
ENST00000543581.5:c.1642A>G	ENSP00000440252.1:p.Thr548Ala
ENST00000559816.1:n.1485A>G
NM_001306146.1:c.1642A>G	NP_001293075.1:p.Thr548Ala
NM_002112.3:c.1741A>G	NP_002103.2:p.Thr581Ala
XM_011521479.1:c.1504A>G	XP_011519781.1:p.Thr502Ala
XM_011521480.1:c.1309A>G	XP_011519782.1:p.Thr437Ala
XM_017022094.1:c.1846A>G	XP_016877583.1:p.Thr616Ala
XM_017022095.1:c.1747A>G	XP_016877584.1:p.Thr583Ala
XM_017022096.1:c.1618A>G	XP_016877585.1:p.Thr540Ala
XM_017022097.1:c.1609A>G	XP_016877586.1:p.Thr537Ala
XM_017022098.1:c.1414A>G	XP_016877587.1:p.Thr472Ala
NM_002112.4:c.1741A>G MANE Select	NP_002103.2:p.Thr581Ala
NM_001306146.2:c.1642A>G	NP_001293075.1:p.Thr548Ala