Canonical Allele Identifier: CA442255514

Gene: PALLD DDX60L

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168512143C>A , CM000666.2:g.168512143C>A	GRCh38
NC_000004.11:g.169433294C>A , CM000666.1:g.169433294C>A	GRCh37
NC_000004.10:g.169669869C>A	NCBI36
NG_013376.1:g.20078C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001166108.2:c.639C>A (PALLD) MANE Select	NP_001159580.1:p.Ala213=
ENST00000505667.6:c.639C>A (PALLD) MANE Select	ENSP00000425556.1:p.Ala213=
NM_001166108.1:c.639C>A (PALLD)	NP_001159580.1:p.Ala213=
NM_016081.3:c.639C>A (PALLD)	NP_057165.3:p.Ala213=
NM_016081.4:c.639C>A (PALLD)	NP_057165.3:p.Ala213=
ENST00000261509.10:c.639C>A (PALLD)	ENSP00000261509.6:p.Ala213=
ENST00000505150.5:n.288+18418G>T (DDX60L)
ENST00000505667.5:c.639C>A (PALLD)	ENSP00000425556.1:p.Ala213=
ENST00000508898.5:c.576C>A (PALLD)	ENSP00000423063.1:p.Ala192=
ENST00000512958.1:n.50-6010G>T (DDX60L)
XM_005262861.3:c.639C>A (PALLD)	XP_005262918.1:p.Ala213=
XM_005262861.4:c.639C>A (PALLD)	XP_005262918.1:p.Ala213=
XM_011531768.1:c.843C>A (PALLD)	XP_011530070.1:p.Ala281=
XM_011531768.2:c.843C>A (PALLD)	XP_011530070.1:p.Ala281=
XM_011531769.1:c.843C>A (PALLD)	XP_011530071.1:p.Ala281=
XM_011531769.2:c.843C>A (PALLD)	XP_011530071.1:p.Ala281=
XM_011531770.1:c.843C>A (PALLD)	XP_011530072.1:p.Ala281=
XM_011531770.2:c.843C>A (PALLD)	XP_011530072.1:p.Ala281=
XM_011531771.1:c.843C>A (PALLD)	XP_011530073.1:p.Ala281=
XM_011531771.2:c.843C>A (PALLD)	XP_011530073.1:p.Ala281=
XM_011531772.1:c.843C>A (PALLD)	XP_011530074.1:p.Ala281=
XM_011531772.2:c.843C>A (PALLD)	XP_011530074.1:p.Ala281=
XM_011531773.1:c.843C>A (PALLD)	XP_011530075.1:p.Ala281=
XM_011531774.1:c.843C>A (PALLD)	XP_011530076.1:p.Ala281=
XM_017007910.1:c.843C>A (PALLD)	XP_016863399.1:p.Ala281=
XM_017007911.1:c.843C>A (PALLD)	XP_016863400.1:p.Ala281=
XR_001741448.2:n.1832+18418G>T