Canonical Allele Identifier: CA10618234

Gene: PALLD CBR4

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.168928086G>A , CM000666.2:g.168928086G>A	GRCh38
NC_000004.11:g.169849237G>A , CM000666.1:g.169849237G>A	GRCh37
NC_000004.10:g.170085812G>A	NCBI36
NG_013376.1:g.436021G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001166108.2:c.*1906G>A (PALLD) MANE Select	NP_001159580.1:n.*1906G>A
ENST00000505667.6:c.*1906G>A (PALLD) MANE Select	ENSP00000425556.1:n.*1906G>A
NM_001166108.1:c.*1906G>A (PALLD)	NP_001159580.1:n.*1906G>A
NM_001166109.1:c.*1701G>A (PALLD)	NP_001159581.1:n.*1701G>A
NM_001166109.2:c.*1701G>A (PALLD)	NP_001159581.1:n.*1701G>A
NM_001166110.1:c.*1701G>A (PALLD)	NP_001159582.1:n.*1701G>A
NM_001166110.2:c.*1701G>A (PALLD)	NP_001159582.1:n.*1701G>A
NM_001367567.1:c.*1906G>A (PALLD)	NP_001354496.1:n.*1906G>A
NM_001367568.1:c.*1701G>A (PALLD)	NP_001354497.1:n.*1701G>A
NM_001367569.1:c.*1701G>A (PALLD)	NP_001354498.1:n.*1701G>A
NM_001367570.1:c.*1906G>A (PALLD)	NP_001354499.1:n.*1906G>A
NM_016081.3:c.*1906G>A (PALLD)	NP_057165.3:n.*1906G>A
NM_016081.4:c.*1906G>A (PALLD)	NP_057165.3:n.*1906G>A
ENST00000261509.10:c.*1906G>A (PALLD)	ENSP00000261509.6:n.*1906G>A
ENST00000507699.1:n.3498G>A (PALLD)
ENST00000507735.5:c.*1701G>A (PALLD)	ENSP00000424016.1:n.*1701G>A
ENST00000507735.6:c.*1701G>A (PALLD)	ENSP00000424016.1:n.*1701G>A
ENST00000509108.1:n.170-33321C>T (CBR4)
ENST00000510042.5:c.*259-33321C>T (CBR4)	ENSP00000424717.1:n.*259-33321C>T
ENST00000704822.1:c.*1701G>A (PALLD)	ENSP00000516055.1:n.*1701G>A
XM_005262861.3:c.*1701G>A (PALLD)	XP_005262918.1:n.*1701G>A
XM_005262861.4:c.*1701G>A (PALLD)	XP_005262918.1:n.*1701G>A
XM_005262866.2:c.*1701G>A (PALLD)	XP_005262923.1:n.*1701G>A
XM_005263315.1:c.536-33321C>T (CBR4)	XP_005263372.1:n.536-33321C>T
XM_005263315.3:c.536-33321C>T (CBR4)	XP_005263372.1:n.536-33321C>T
XM_011531768.1:c.*1701G>A (PALLD)	XP_011530070.1:n.*1701G>A
XM_011531768.2:c.*1701G>A (PALLD)	XP_011530070.1:n.*1701G>A
XM_011531769.1:c.*1701G>A (PALLD)	XP_011530071.1:n.*1701G>A
XM_011531769.2:c.*1701G>A (PALLD)	XP_011530071.1:n.*1701G>A
XM_011531770.1:c.*1906G>A (PALLD)	XP_011530072.1:n.*1906G>A
XM_011531770.2:c.*1906G>A (PALLD)	XP_011530072.1:n.*1906G>A
XM_011531771.1:c.*1701G>A (PALLD)	XP_011530073.1:n.*1701G>A
XM_011531771.2:c.*1701G>A (PALLD)	XP_011530073.1:n.*1701G>A
XM_011531772.1:c.*1701G>A (PALLD)	XP_011530074.1:n.*1701G>A
XM_011531772.2:c.*1701G>A (PALLD)	XP_011530074.1:n.*1701G>A
XM_011531773.1:c.*1701G>A (PALLD)	XP_011530075.1:n.*1701G>A
XM_011531774.1:c.*1701G>A (PALLD)	XP_011530076.1:n.*1701G>A
XM_011531775.1:c.*1701G>A (PALLD)	XP_011530077.1:n.*1701G>A
XM_011531776.1:c.*1701G>A (PALLD)	XP_011530078.1:n.*1701G>A
XM_017007910.1:c.*1906G>A (PALLD)	XP_016863399.1:n.*1906G>A
XM_017008782.1:c.566-33321C>T (CBR4)	XP_016864271.1:n.566-33321C>T
XM_017008783.2:c.*566C>T (CBR4)	XP_016864272.1:n.*566C>T
XM_024453939.1:c.*1701G>A (PALLD)	XP_024309707.1:n.*1701G>A
XM_024453940.1:c.*1701G>A (PALLD)	XP_024309708.1:n.*1701G>A
XR_001741341.1:n.901+451C>T (CBR4)
XR_938789.1:n.901+451C>T (CBR4)