Canonical Allele Identifier: CA392377108

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534677A>G (hg19) ; chr15:g.50242480A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242480A>G , CM000677.2:g.50242480A>G	GRCh38
NC_000015.9:g.50534677A>G , CM000677.1:g.50534677A>G	GRCh37
NC_000015.8:g.48321969A>G	NCBI36
NG_027487.1:g.28486T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1769T>C MANE Select	ENSP00000267845.3:p.Val590Ala
ENST00000267845.7:c.1769T>C	ENSP00000267845.3:p.Val590Ala
ENST00000543581.5:c.1670T>C	ENSP00000440252.1:p.Val557Ala
ENST00000559816.1:n.1513T>C
NM_001306146.1:c.1670T>C	NP_001293075.1:p.Val557Ala
NM_002112.3:c.1769T>C	NP_002103.2:p.Val590Ala
XM_011521479.1:c.1532T>C	XP_011519781.1:p.Val511Ala
XM_011521480.1:c.1337T>C	XP_011519782.1:p.Val446Ala
XM_017022094.1:c.1874T>C	XP_016877583.1:p.Val625Ala
XM_017022095.1:c.1775T>C	XP_016877584.1:p.Val592Ala
XM_017022096.1:c.1646T>C	XP_016877585.1:p.Val549Ala
XM_017022097.1:c.1637T>C	XP_016877586.1:p.Val546Ala
XM_017022098.1:c.1442T>C	XP_016877587.1:p.Val481Ala
NM_002112.4:c.1769T>C MANE Select	NP_002103.2:p.Val590Ala
NM_001306146.2:c.1670T>C	NP_001293075.1:p.Val557Ala