Canonical Allele Identifier: CA392376905

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534579T>G (hg19) ; chr15:g.50242382T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242382T>G , CM000677.2:g.50242382T>G	GRCh38
NC_000015.9:g.50534579T>G , CM000677.1:g.50534579T>G	GRCh37
NC_000015.8:g.48321871T>G	NCBI36
NG_027487.1:g.28584A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1867A>C MANE Select	ENSP00000267845.3:p.Met623Leu
ENST00000267845.7:c.1867A>C	ENSP00000267845.3:p.Met623Leu
ENST00000543581.5:c.1768A>C	ENSP00000440252.1:p.Met590Leu
ENST00000559816.1:n.1611A>C
NM_001306146.1:c.1768A>C	NP_001293075.1:p.Met590Leu
NM_002112.3:c.1867A>C	NP_002103.2:p.Met623Leu
XM_011521479.1:c.1630A>C	XP_011519781.1:p.Met544Leu
XM_011521480.1:c.1435A>C	XP_011519782.1:p.Met479Leu
XM_017022094.1:c.1972A>C	XP_016877583.1:p.Met658Leu
XM_017022095.1:c.1873A>C	XP_016877584.1:p.Met625Leu
XM_017022096.1:c.1744A>C	XP_016877585.1:p.Met582Leu
XM_017022097.1:c.1735A>C	XP_016877586.1:p.Met579Leu
XM_017022098.1:c.1540A>C	XP_016877587.1:p.Met514Leu
NM_002112.4:c.1867A>C MANE Select	NP_002103.2:p.Met623Leu
NM_001306146.2:c.1768A>C	NP_001293075.1:p.Met590Leu