Canonical Allele Identifier: CA392376917

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534584T>A (hg19) ; chr15:g.50242387T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242387T>A , CM000677.2:g.50242387T>A	GRCh38
NC_000015.9:g.50534584T>A , CM000677.1:g.50534584T>A	GRCh37
NC_000015.8:g.48321876T>A	NCBI36
NG_027487.1:g.28579A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1862A>T MANE Select	ENSP00000267845.3:p.Asp621Val
ENST00000267845.7:c.1862A>T	ENSP00000267845.3:p.Asp621Val
ENST00000543581.5:c.1763A>T	ENSP00000440252.1:p.Asp588Val
ENST00000559816.1:n.1606A>T
NM_001306146.1:c.1763A>T	NP_001293075.1:p.Asp588Val
NM_002112.3:c.1862A>T	NP_002103.2:p.Asp621Val
XM_011521479.1:c.1625A>T	XP_011519781.1:p.Asp542Val
XM_011521480.1:c.1430A>T	XP_011519782.1:p.Asp477Val
XM_017022094.1:c.1967A>T	XP_016877583.1:p.Asp656Val
XM_017022095.1:c.1868A>T	XP_016877584.1:p.Asp623Val
XM_017022096.1:c.1739A>T	XP_016877585.1:p.Asp580Val
XM_017022097.1:c.1730A>T	XP_016877586.1:p.Asp577Val
XM_017022098.1:c.1535A>T	XP_016877587.1:p.Asp512Val
NM_002112.4:c.1862A>T MANE Select	NP_002103.2:p.Asp621Val
NM_001306146.2:c.1763A>T	NP_001293075.1:p.Asp588Val