Canonical Allele Identifier: CA2672625649

Gene: PALLD RPL9P16

Linked Data

• gnomAD v4: 4-168756217-T-TTTTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168756217_168756218insTTTTTG , CM000666.2:g.168756217_168756218insTTTTTG	GRCh38
NC_000004.11:g.169677368_169677369insTTTTTG , CM000666.1:g.169677368_169677369insTTTTTG	GRCh37
NC_000004.10:g.169913943_169913944insTTTTTG	NCBI36
NG_013376.1:g.264152_264153insTTTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505667.6:c.1964+44294_1964+44295insTTTTTG (PALLD) MANE Select	ENSP00000425556.1:n.1964+44294_1964+44295insTTTTTG
ENST00000649826.1:c.343+44294_343+44295insTTTTTG (PALLD)
ENST00000261509.10:c.1964+44294_1964+44295insTTTTTG (PALLD)	ENSP00000261509.6:n.1964+44294_1964+44295insTTTTTG
ENST00000491923.1:n.402_403insTTTTTG (RPL9P16)
ENST00000505667.5:c.1964+44294_1964+44295insTTTTTG (PALLD)	ENSP00000425556.1:n.1964+44294_1964+44295insTTTTTG
ENST00000510998.5:c.-158+43943_-158+43944insTTTTTG (PALLD)	ENSP00000422135.1:n.-158+43943_-158+43944insTTTTTG
ENST00000512127.5:c.818+44294_818+44295insTTTTTG (PALLD)	ENSP00000426947.1:n.818+44294_818+44295insTTTTTG
NM_001166108.1:c.1964+44294_1964+44295insTTTTTG (PALLD)	NP_001159580.1:n.1964+44294_1964+44295insTTTTTG
NM_001166109.1:c.818+44294_818+44295insTTTTTG (PALLD)	NP_001159581.1:n.818+44294_818+44295insTTTTTG
NM_016081.3:c.1964+44294_1964+44295insTTTTTG (PALLD)	NP_057165.3:n.1964+44294_1964+44295insTTTTTG
XM_005262861.3:c.1964+44294_1964+44295insTTTTTG (PALLD)	XP_005262918.1:n.1964+44294_1964+44295insTTTTTG
XM_005262866.2:c.818+44294_818+44295insTTTTTG (PALLD)	XP_005262923.1:n.818+44294_818+44295insTTTTTG
XM_011531768.1:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530070.1:n.2168+44294_2168+44295insTTTTTG
XM_011531769.1:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530071.1:n.2168+44294_2168+44295insTTTTTG
XM_011531770.1:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530072.1:n.2168+44294_2168+44295insTTTTTG
XM_011531771.1:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530073.1:n.2168+44294_2168+44295insTTTTTG
XM_011531772.1:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530074.1:n.2168+44294_2168+44295insTTTTTG
XM_011531773.1:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530075.1:n.2168+44294_2168+44295insTTTTTG
XM_011531774.1:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530076.1:n.2168+44294_2168+44295insTTTTTG
XM_011531775.1:c.818+44294_818+44295insTTTTTG (PALLD)	XP_011530077.1:n.818+44294_818+44295insTTTTTG
XM_011531776.1:c.818+44294_818+44295insTTTTTG (PALLD)	XP_011530078.1:n.818+44294_818+44295insTTTTTG
XM_005262861.4:c.1964+44294_1964+44295insTTTTTG (PALLD)	XP_005262918.1:n.1964+44294_1964+44295insTTTTTG
XM_011531768.2:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530070.1:n.2168+44294_2168+44295insTTTTTG
XM_011531769.2:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530071.1:n.2168+44294_2168+44295insTTTTTG
XM_011531770.2:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530072.1:n.2168+44294_2168+44295insTTTTTG
XM_011531771.2:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530073.1:n.2168+44294_2168+44295insTTTTTG
XM_011531772.2:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_011530074.1:n.2168+44294_2168+44295insTTTTTG
XM_017007910.1:c.2168+44294_2168+44295insTTTTTG (PALLD)	XP_016863399.1:n.2168+44294_2168+44295insTTTTTG
XM_024453939.1:c.818+44294_818+44295insTTTTTG (PALLD)	XP_024309707.1:n.818+44294_818+44295insTTTTTG
NM_001166108.2:c.1964+44294_1964+44295insTTTTTG (PALLD) MANE Select	NP_001159580.1:n.1964+44294_1964+44295insTTTTTG
NM_001166109.2:c.818+44294_818+44295insTTTTTG (PALLD)	NP_001159581.1:n.818+44294_818+44295insTTTTTG
NM_016081.4:c.1964+44294_1964+44295insTTTTTG (PALLD)	NP_057165.3:n.1964+44294_1964+44295insTTTTTG