Canonical Allele Identifier: CA392377272

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534753G>T (hg19) ; chr15:g.50242556G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242556G>T , CM000677.2:g.50242556G>T	GRCh38
NC_000015.9:g.50534753G>T , CM000677.1:g.50534753G>T	GRCh37
NC_000015.8:g.48322045G>T	NCBI36
NG_027487.1:g.28410C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1693C>A MANE Select	ENSP00000267845.3:p.Leu565Met
ENST00000267845.7:c.1693C>A	ENSP00000267845.3:p.Leu565Met
ENST00000543581.5:c.1594C>A	ENSP00000440252.1:p.Leu532Met
ENST00000559816.1:n.1437C>A
NM_001306146.1:c.1594C>A	NP_001293075.1:p.Leu532Met
NM_002112.3:c.1693C>A	NP_002103.2:p.Leu565Met
XM_011521479.1:c.1456C>A	XP_011519781.1:p.Leu486Met
XM_011521480.1:c.1261C>A	XP_011519782.1:p.Leu421Met
XM_017022094.1:c.1798C>A	XP_016877583.1:p.Leu600Met
XM_017022095.1:c.1699C>A	XP_016877584.1:p.Leu567Met
XM_017022096.1:c.1570C>A	XP_016877585.1:p.Leu524Met
XM_017022097.1:c.1561C>A	XP_016877586.1:p.Leu521Met
XM_017022098.1:c.1366C>A	XP_016877587.1:p.Leu456Met
NM_002112.4:c.1693C>A MANE Select	NP_002103.2:p.Leu565Met
NM_001306146.2:c.1594C>A	NP_001293075.1:p.Leu532Met