Canonical Allele Identifier: CA392377068

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534657G>A (hg19) ; chr15:g.50242460G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242460G>A , CM000677.2:g.50242460G>A	GRCh38
NC_000015.9:g.50534657G>A , CM000677.1:g.50534657G>A	GRCh37
NC_000015.8:g.48321949G>A	NCBI36
NG_027487.1:g.28506C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1789C>T MANE Select	ENSP00000267845.3:p.Pro597Ser
ENST00000267845.7:c.1789C>T	ENSP00000267845.3:p.Pro597Ser
ENST00000543581.5:c.1690C>T	ENSP00000440252.1:p.Pro564Ser
ENST00000559816.1:n.1533C>T
NM_001306146.1:c.1690C>T	NP_001293075.1:p.Pro564Ser
NM_002112.3:c.1789C>T	NP_002103.2:p.Pro597Ser
XM_011521479.1:c.1552C>T	XP_011519781.1:p.Pro518Ser
XM_011521480.1:c.1357C>T	XP_011519782.1:p.Pro453Ser
XM_017022094.1:c.1894C>T	XP_016877583.1:p.Pro632Ser
XM_017022095.1:c.1795C>T	XP_016877584.1:p.Pro599Ser
XM_017022096.1:c.1666C>T	XP_016877585.1:p.Pro556Ser
XM_017022097.1:c.1657C>T	XP_016877586.1:p.Pro553Ser
XM_017022098.1:c.1462C>T	XP_016877587.1:p.Pro488Ser
NM_002112.4:c.1789C>T MANE Select	NP_002103.2:p.Pro597Ser
NM_001306146.2:c.1690C>T	NP_001293075.1:p.Pro564Ser