Canonical Allele Identifier: CA392376912

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534582T>G (hg19) ; chr15:g.50242385T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242385T>G , CM000677.2:g.50242385T>G	GRCh38
NC_000015.9:g.50534582T>G , CM000677.1:g.50534582T>G	GRCh37
NC_000015.8:g.48321874T>G	NCBI36
NG_027487.1:g.28581A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1864A>C MANE Select	ENSP00000267845.3:p.Met622Leu
ENST00000267845.7:c.1864A>C	ENSP00000267845.3:p.Met622Leu
ENST00000543581.5:c.1765A>C	ENSP00000440252.1:p.Met589Leu
ENST00000559816.1:n.1608A>C
NM_001306146.1:c.1765A>C	NP_001293075.1:p.Met589Leu
NM_002112.3:c.1864A>C	NP_002103.2:p.Met622Leu
XM_011521479.1:c.1627A>C	XP_011519781.1:p.Met543Leu
XM_011521480.1:c.1432A>C	XP_011519782.1:p.Met478Leu
XM_017022094.1:c.1969A>C	XP_016877583.1:p.Met657Leu
XM_017022095.1:c.1870A>C	XP_016877584.1:p.Met624Leu
XM_017022096.1:c.1741A>C	XP_016877585.1:p.Met581Leu
XM_017022097.1:c.1732A>C	XP_016877586.1:p.Met578Leu
XM_017022098.1:c.1537A>C	XP_016877587.1:p.Met513Leu
NM_002112.4:c.1864A>C MANE Select	NP_002103.2:p.Met622Leu
NM_001306146.2:c.1765A>C	NP_001293075.1:p.Met589Leu