Canonical Allele Identifier: CA2213431620

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23636022_23636024delinsCTT , CM000678.2:g.23636022_23636024delinsCTT	GRCh38
NC_000016.9:g.23647343_23647345delinsCTT , CM000678.1:g.23647343_23647345delinsCTT	GRCh37
NC_000016.8:g.23554844_23554846delinsCTT	NCBI36
NG_007406.1:g.10334_10336delinsAAG , LRG_308:g.10334_10336delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.528_530delinsAAG	ENSP00000460666.3:p.Lys176=
ENST00000565038.2:c.211+1826_211+1828delinsAAG	ENSP00000459882.2:n.211+1826_211+1828delinsAAG
ENST00000566069.6:c.522_524delinsAAG	ENSP00000459237.2:p.Lys174=
ENST00000697377.2:c.528_530delinsAAG	ENSP00000513286.2:p.Lys176=
ENST00000697379.2:c.528_530delinsAAG	ENSP00000513287.2:p.Lys176=
ENST00000561514.2:c.-364_-362delinsAAG	ENSP00000460666.2:n.-364_-362delinsAAG
ENST00000697374.1:c.-364_-362delinsAAG	ENSP00000513284.1:n.-364_-362delinsAAG
ENST00000697375.1:n.1869_1871delinsAAG
ENST00000697376.1:c.-364_-362delinsAAG	ENSP00000513285.1:n.-364_-362delinsAAG
ENST00000697377.1:c.-364_-362delinsAAG	ENSP00000513286.1:n.-364_-362delinsAAG
ENST00000697378.1:n.1042_1044delinsAAG
ENST00000697379.1:c.-364_-362delinsAAG	ENSP00000513287.1:n.-364_-362delinsAAG
ENST00000697382.1:c.-364_-362delinsAAG	ENSP00000513288.1:n.-364_-362delinsAAG
ENST00000697383.1:c.48+5086_48+5088delinsAAG	ENSP00000513289.1:n.48+5086_48+5088delinsAAG
ENST00000697384.1:n.676_678delinsAAG
ENST00000261584.9:c.522_524delinsAAG MANE Select	ENSP00000261584.4:p.Lys174=
ENST00000261584.8:c.522_524delinsAAG	ENSP00000261584.4:p.Lys174=
ENST00000565038.1:c.86+1826_86+1828delinsAAG
ENST00000568219.5:c.-364_-362delinsAAG	ENSP00000454703.2:n.-364_-362delinsAAG
NM_024675.3:c.522_524delinsAAG , LRG_308t1:c.522_524delinsAAG	NP_078951.2:p.Lys174=
XM_011545946.1:c.528_530delinsAAG	XP_011544248.1:p.Lys176=
XM_011545947.1:c.528_530delinsAAG	XP_011544249.1:p.Lys176=
XM_011545948.1:c.-364_-362delinsAAG	XP_011544250.1:n.-364_-362delinsAAG
XR_950851.1:n.1318_1320delinsAAG
XM_011545946.2:c.528_530delinsAAG	XP_011544248.1:p.Lys176=
XM_011545947.2:c.528_530delinsAAG	XP_011544249.1:p.Lys176=
XM_011545948.2:c.-364_-362delinsAAG	XP_011544250.1:n.-364_-362delinsAAG
XM_017023671.1:c.528_530delinsAAG	XP_016879160.1:p.Lys176=
XM_017023672.2:c.522_524delinsAAG	XP_016879161.1:p.Lys174=
XM_017023673.2:c.522_524delinsAAG	XP_016879162.1:p.Lys174=
NM_024675.4:c.522_524delinsAAG MANE Select	NP_078951.2:p.Lys174=