Canonical Allele Identifier: CA392377031

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534638G>T (hg19) ; chr15:g.50242441G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242441G>T , CM000677.2:g.50242441G>T	GRCh38
NC_000015.9:g.50534638G>T , CM000677.1:g.50534638G>T	GRCh37
NC_000015.8:g.48321930G>T	NCBI36
NG_027487.1:g.28525C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1808C>A MANE Select	ENSP00000267845.3:p.Ser603Tyr
ENST00000267845.7:c.1808C>A	ENSP00000267845.3:p.Ser603Tyr
ENST00000543581.5:c.1709C>A	ENSP00000440252.1:p.Ser570Tyr
ENST00000559816.1:n.1552C>A
NM_001306146.1:c.1709C>A	NP_001293075.1:p.Ser570Tyr
NM_002112.3:c.1808C>A	NP_002103.2:p.Ser603Tyr
XM_011521479.1:c.1571C>A	XP_011519781.1:p.Ser524Tyr
XM_011521480.1:c.1376C>A	XP_011519782.1:p.Ser459Tyr
XM_017022094.1:c.1913C>A	XP_016877583.1:p.Ser638Tyr
XM_017022095.1:c.1814C>A	XP_016877584.1:p.Ser605Tyr
XM_017022096.1:c.1685C>A	XP_016877585.1:p.Ser562Tyr
XM_017022097.1:c.1676C>A	XP_016877586.1:p.Ser559Tyr
XM_017022098.1:c.1481C>A	XP_016877587.1:p.Ser494Tyr
NM_002112.4:c.1808C>A MANE Select	NP_002103.2:p.Ser603Tyr
NM_001306146.2:c.1709C>A	NP_001293075.1:p.Ser570Tyr