Canonical Allele Identifier: CA358793801

Gene: PALLD

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168668292C>G , CM000666.2:g.168668292C>G	GRCh38
NC_000004.11:g.169589443C>G , CM000666.1:g.169589443C>G	GRCh37
NC_000004.10:g.169826018C>G	NCBI36
NG_013376.1:g.176227C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001166108.2:c.1011C>G MANE Select	NP_001159580.1:p.Asp337Glu
ENST00000505667.6:c.1011C>G MANE Select	ENSP00000425556.1:p.Asp337Glu
NM_001166108.1:c.1011C>G	NP_001159580.1:p.Asp337Glu
NM_001166109.1:c.-136C>G	NP_001159581.1:n.-136C>G
NM_001166109.2:c.-136C>G	NP_001159581.1:n.-136C>G
NM_016081.3:c.1011C>G	NP_057165.3:p.Asp337Glu
NM_016081.4:c.1011C>G	NP_057165.3:p.Asp337Glu
ENST00000261509.10:c.1011C>G	ENSP00000261509.6:p.Asp337Glu
ENST00000503457.1:c.-136C>G	ENSP00000424288.1:n.-136C>G
ENST00000504519.5:c.-208-9608C>G	ENSP00000424121.1:n.-208-9608C>G
ENST00000505667.5:c.1011C>G	ENSP00000425556.1:p.Asp337Glu
ENST00000508898.5:c.948C>G	ENSP00000423063.1:p.Asp316Glu
ENST00000512127.5:c.-136C>G	ENSP00000426947.1:n.-136C>G
ENST00000513245.5:c.-136C>G	ENSP00000422016.1:n.-136C>G
XM_005262861.3:c.1011C>G	XP_005262918.1:p.Asp337Glu
XM_005262861.4:c.1011C>G	XP_005262918.1:p.Asp337Glu
XM_005262866.2:c.-136C>G	XP_005262923.1:n.-136C>G
XM_011531768.1:c.1215C>G	XP_011530070.1:p.Asp405Glu
XM_011531768.2:c.1215C>G	XP_011530070.1:p.Asp405Glu
XM_011531769.1:c.1215C>G	XP_011530071.1:p.Asp405Glu
XM_011531769.2:c.1215C>G	XP_011530071.1:p.Asp405Glu
XM_011531770.1:c.1215C>G	XP_011530072.1:p.Asp405Glu
XM_011531770.2:c.1215C>G	XP_011530072.1:p.Asp405Glu
XM_011531771.1:c.1215C>G	XP_011530073.1:p.Asp405Glu
XM_011531771.2:c.1215C>G	XP_011530073.1:p.Asp405Glu
XM_011531772.1:c.1215C>G	XP_011530074.1:p.Asp405Glu
XM_011531772.2:c.1215C>G	XP_011530074.1:p.Asp405Glu
XM_011531773.1:c.1215C>G	XP_011530075.1:p.Asp405Glu
XM_011531774.1:c.1215C>G	XP_011530076.1:p.Asp405Glu
XM_011531775.1:c.-136C>G	XP_011530077.1:n.-136C>G
XM_011531776.1:c.-136C>G	XP_011530078.1:n.-136C>G
XM_017007910.1:c.1215C>G	XP_016863399.1:p.Asp405Glu
XM_017007911.1:c.1215C>G	XP_016863400.1:p.Asp405Glu
XM_024453939.1:c.-136C>G	XP_024309707.1:n.-136C>G
XR_939428.1:n.493+1369G>C