Canonical Allele Identifier: CA392377232

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534734C>G (hg19) ; chr15:g.50242537C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242537C>G , CM000677.2:g.50242537C>G	GRCh38
NC_000015.9:g.50534734C>G , CM000677.1:g.50534734C>G	GRCh37
NC_000015.8:g.48322026C>G	NCBI36
NG_027487.1:g.28429G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1712G>C MANE Select	ENSP00000267845.3:p.Ser571Thr
ENST00000267845.7:c.1712G>C	ENSP00000267845.3:p.Ser571Thr
ENST00000543581.5:c.1613G>C	ENSP00000440252.1:p.Ser538Thr
ENST00000559816.1:n.1456G>C
NM_001306146.1:c.1613G>C	NP_001293075.1:p.Ser538Thr
NM_002112.3:c.1712G>C	NP_002103.2:p.Ser571Thr
XM_011521479.1:c.1475G>C	XP_011519781.1:p.Ser492Thr
XM_011521480.1:c.1280G>C	XP_011519782.1:p.Ser427Thr
XM_017022094.1:c.1817G>C	XP_016877583.1:p.Ser606Thr
XM_017022095.1:c.1718G>C	XP_016877584.1:p.Ser573Thr
XM_017022096.1:c.1589G>C	XP_016877585.1:p.Ser530Thr
XM_017022097.1:c.1580G>C	XP_016877586.1:p.Ser527Thr
XM_017022098.1:c.1385G>C	XP_016877587.1:p.Ser462Thr
NM_002112.4:c.1712G>C MANE Select	NP_002103.2:p.Ser571Thr
NM_001306146.2:c.1613G>C	NP_001293075.1:p.Ser538Thr