Canonical Allele Identifier: CA392377277

Gene: HDC

Linked Data

• COSMIC: COSM962534
• MyVariant Identifiers: chr15:g.50534755T>C (hg19) ; chr15:g.50242558T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242558T>C , CM000677.2:g.50242558T>C	GRCh38
NC_000015.9:g.50534755T>C , CM000677.1:g.50534755T>C	GRCh37
NC_000015.8:g.48322047T>C	NCBI36
NG_027487.1:g.28408A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1691A>G MANE Select	ENSP00000267845.3:p.Lys564Arg
ENST00000267845.7:c.1691A>G	ENSP00000267845.3:p.Lys564Arg
ENST00000543581.5:c.1592A>G	ENSP00000440252.1:p.Lys531Arg
ENST00000559816.1:n.1435A>G
NM_001306146.1:c.1592A>G	NP_001293075.1:p.Lys531Arg
NM_002112.3:c.1691A>G	NP_002103.2:p.Lys564Arg
XM_011521479.1:c.1454A>G	XP_011519781.1:p.Lys485Arg
XM_011521480.1:c.1259A>G	XP_011519782.1:p.Lys420Arg
XM_017022094.1:c.1796A>G	XP_016877583.1:p.Lys599Arg
XM_017022095.1:c.1697A>G	XP_016877584.1:p.Lys566Arg
XM_017022096.1:c.1568A>G	XP_016877585.1:p.Lys523Arg
XM_017022097.1:c.1559A>G	XP_016877586.1:p.Lys520Arg
XM_017022098.1:c.1364A>G	XP_016877587.1:p.Lys455Arg
NM_002112.4:c.1691A>G MANE Select	NP_002103.2:p.Lys564Arg
NM_001306146.2:c.1592A>G	NP_001293075.1:p.Lys531Arg