Canonical Allele Identifier: CA392376904

Gene: HDC

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1867A>G MANE Select	ENSP00000267845.3:p.Met623Val
ENST00000267845.7:c.1867A>G	ENSP00000267845.3:p.Met623Val
ENST00000543581.5:c.1768A>G	ENSP00000440252.1:p.Met590Val
ENST00000559816.1:n.1611A>G
NM_001306146.1:c.1768A>G	NP_001293075.1:p.Met590Val
NM_002112.3:c.1867A>G	NP_002103.2:p.Met623Val
XM_011521479.1:c.1630A>G	XP_011519781.1:p.Met544Val
XM_011521480.1:c.1435A>G	XP_011519782.1:p.Met479Val
XM_017022094.1:c.1972A>G	XP_016877583.1:p.Met658Val
XM_017022095.1:c.1873A>G	XP_016877584.1:p.Met625Val
XM_017022096.1:c.1744A>G	XP_016877585.1:p.Met582Val
XM_017022097.1:c.1735A>G	XP_016877586.1:p.Met579Val
XM_017022098.1:c.1540A>G	XP_016877587.1:p.Met514Val
NM_002112.4:c.1867A>G MANE Select	NP_002103.2:p.Met623Val
NM_001306146.2:c.1768A>G	NP_001293075.1:p.Met590Val