Canonical Allele Identifier: CA490314105

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534664A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242467A>G , CM000677.2:g.50242467A>G	GRCh38
NC_000015.9:g.50534664A>G , CM000677.1:g.50534664A>G	GRCh37
NC_000015.8:g.48321956A>G	NCBI36
NG_027487.1:g.28499T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1782T>C MANE Select	ENSP00000267845.3:p.Ala594=
ENST00000267845.7:c.1782T>C	ENSP00000267845.3:p.Ala594=
ENST00000543581.5:c.1683T>C	ENSP00000440252.1:p.Ala561=
ENST00000559816.1:n.1526T>C
NM_001306146.1:c.1683T>C	NP_001293075.1:p.Ala561=
NM_002112.3:c.1782T>C	NP_002103.2:p.Ala594=
XM_011521479.1:c.1545T>C	XP_011519781.1:p.Ala515=
XM_011521480.1:c.1350T>C	XP_011519782.1:p.Ala450=
XM_017022094.1:c.1887T>C	XP_016877583.1:p.Ala629=
XM_017022095.1:c.1788T>C	XP_016877584.1:p.Ala596=
XM_017022096.1:c.1659T>C	XP_016877585.1:p.Ala553=
XM_017022097.1:c.1650T>C	XP_016877586.1:p.Ala550=
XM_017022098.1:c.1455T>C	XP_016877587.1:p.Ala485=
NM_002112.4:c.1782T>C MANE Select	NP_002103.2:p.Ala594=
NM_001306146.2:c.1683T>C	NP_001293075.1:p.Ala561=