Canonical Allele Identifier: CA392376935

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534592A>C (hg19) ; chr15:g.50242395A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242395A>C , CM000677.2:g.50242395A>C	GRCh38
NC_000015.9:g.50534592A>C , CM000677.1:g.50534592A>C	GRCh37
NC_000015.8:g.48321884A>C	NCBI36
NG_027487.1:g.28571T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1854T>G MANE Select	ENSP00000267845.3:p.Phe618Leu
ENST00000267845.7:c.1854T>G	ENSP00000267845.3:p.Phe618Leu
ENST00000543581.5:c.1755T>G	ENSP00000440252.1:p.Phe585Leu
ENST00000559816.1:n.1598T>G
NM_001306146.1:c.1755T>G	NP_001293075.1:p.Phe585Leu
NM_002112.3:c.1854T>G	NP_002103.2:p.Phe618Leu
XM_011521479.1:c.1617T>G	XP_011519781.1:p.Phe539Leu
XM_011521480.1:c.1422T>G	XP_011519782.1:p.Phe474Leu
XM_017022094.1:c.1959T>G	XP_016877583.1:p.Phe653Leu
XM_017022095.1:c.1860T>G	XP_016877584.1:p.Phe620Leu
XM_017022096.1:c.1731T>G	XP_016877585.1:p.Phe577Leu
XM_017022097.1:c.1722T>G	XP_016877586.1:p.Phe574Leu
XM_017022098.1:c.1527T>G	XP_016877587.1:p.Phe509Leu
NM_002112.4:c.1854T>G MANE Select	NP_002103.2:p.Phe618Leu
NM_001306146.2:c.1755T>G	NP_001293075.1:p.Phe585Leu