Canonical Allele Identifier: CA392377064

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534654G>T (hg19) ; chr15:g.50242457G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242457G>T , CM000677.2:g.50242457G>T	GRCh38
NC_000015.9:g.50534654G>T , CM000677.1:g.50534654G>T	GRCh37
NC_000015.8:g.48321946G>T	NCBI36
NG_027487.1:g.28509C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1792C>A MANE Select	ENSP00000267845.3:p.Leu598Met
ENST00000267845.7:c.1792C>A	ENSP00000267845.3:p.Leu598Met
ENST00000543581.5:c.1693C>A	ENSP00000440252.1:p.Leu565Met
ENST00000559816.1:n.1536C>A
NM_001306146.1:c.1693C>A	NP_001293075.1:p.Leu565Met
NM_002112.3:c.1792C>A	NP_002103.2:p.Leu598Met
XM_011521479.1:c.1555C>A	XP_011519781.1:p.Leu519Met
XM_011521480.1:c.1360C>A	XP_011519782.1:p.Leu454Met
XM_017022094.1:c.1897C>A	XP_016877583.1:p.Leu633Met
XM_017022095.1:c.1798C>A	XP_016877584.1:p.Leu600Met
XM_017022096.1:c.1669C>A	XP_016877585.1:p.Leu557Met
XM_017022097.1:c.1660C>A	XP_016877586.1:p.Leu554Met
XM_017022098.1:c.1465C>A	XP_016877587.1:p.Leu489Met
NM_002112.4:c.1792C>A MANE Select	NP_002103.2:p.Leu598Met
NM_001306146.2:c.1693C>A	NP_001293075.1:p.Leu565Met