Canonical Allele Identifier: CA392377291

Gene: HDC

Linked Data

• MyVariant Identifiers: chr15:g.50534761T>A (hg19) ; chr15:g.50242564T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.50242564T>A , CM000677.2:g.50242564T>A	GRCh38
NC_000015.9:g.50534761T>A , CM000677.1:g.50534761T>A	GRCh37
NC_000015.8:g.48322053T>A	NCBI36
NG_027487.1:g.28402A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267845.8:c.1685A>T MANE Select	ENSP00000267845.3:p.Lys562Met
ENST00000267845.7:c.1685A>T	ENSP00000267845.3:p.Lys562Met
ENST00000543581.5:c.1586A>T	ENSP00000440252.1:p.Lys529Met
ENST00000559816.1:n.1429A>T
NM_001306146.1:c.1586A>T	NP_001293075.1:p.Lys529Met
NM_002112.3:c.1685A>T	NP_002103.2:p.Lys562Met
XM_011521479.1:c.1448A>T	XP_011519781.1:p.Lys483Met
XM_011521480.1:c.1253A>T	XP_011519782.1:p.Lys418Met
XM_017022094.1:c.1790A>T	XP_016877583.1:p.Lys597Met
XM_017022095.1:c.1691A>T	XP_016877584.1:p.Lys564Met
XM_017022096.1:c.1562A>T	XP_016877585.1:p.Lys521Met
XM_017022097.1:c.1553A>T	XP_016877586.1:p.Lys518Met
XM_017022098.1:c.1358A>T	XP_016877587.1:p.Lys453Met
NM_002112.4:c.1685A>T MANE Select	NP_002103.2:p.Lys562Met
NM_001306146.2:c.1586A>T	NP_001293075.1:p.Lys529Met