Canonical Allele Identifier: CA2213409441

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23621222_23621225delinsAAAC , CM000678.2:g.23621222_23621225delinsAAAC	GRCh38
NC_000016.9:g.23632543_23632546delinsAAAC , CM000678.1:g.23632543_23632546delinsAAAC	GRCh37
NC_000016.8:g.23540044_23540047delinsAAAC	NCBI36
NG_007406.1:g.25133_25136delinsGTTT , LRG_308:g.25133_25136delinsGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3119+137_3119+140delinsGTTT	ENSP00000460666.3:n.3119+137_3119+140delinsGTTT
ENST00000565038.2:c.*594+137_*594+140delinsGTTT	ENSP00000459882.2:n.*594+137_*594+140delinsGTTT
ENST00000566069.6:c.3113+137_3113+140delinsGTTT	ENSP00000459237.2:n.3113+137_3113+140delinsGTTT
ENST00000697377.2:c.2957+137_2957+140delinsGTTT	ENSP00000513286.2:n.2957+137_2957+140delinsGTTT
ENST00000697379.2:c.3119+137_3119+140delinsGTTT	ENSP00000513287.2:n.3119+137_3119+140delinsGTTT
ENST00000561514.2:c.2228+137_2228+140delinsGTTT	ENSP00000460666.2:n.2228+137_2228+140delinsGTTT
ENST00000697374.1:c.2228+137_2228+140delinsGTTT	ENSP00000513284.1:n.2228+137_2228+140delinsGTTT
ENST00000697375.1:n.4460+137_4460+140delinsGTTT
ENST00000697376.1:c.2228+137_2228+140delinsGTTT	ENSP00000513285.1:n.2228+137_2228+140delinsGTTT
ENST00000697377.1:c.2066+137_2066+140delinsGTTT	ENSP00000513286.1:n.2066+137_2066+140delinsGTTT
ENST00000697378.1:n.3633+137_3633+140delinsGTTT
ENST00000697379.1:c.2228+137_2228+140delinsGTTT	ENSP00000513287.1:n.2228+137_2228+140delinsGTTT
ENST00000697380.1:n.2405+137_2405+140delinsGTTT
ENST00000697381.1:n.1808+137_1808+140delinsGTTT
ENST00000697382.1:c.2228+137_2228+140delinsGTTT	ENSP00000513288.1:n.2228+137_2228+140delinsGTTT
ENST00000697383.1:c.647+137_647+140delinsGTTT	ENSP00000513289.1:n.647+137_647+140delinsGTTT
ENST00000261584.9:c.3113+137_3113+140delinsGTTT MANE Select	ENSP00000261584.4:n.3113+137_3113+140delinsGTTT
ENST00000261584.8:c.3113+137_3113+140delinsGTTT	ENSP00000261584.4:n.3113+137_3113+140delinsGTTT
ENST00000566069.5:c.28+137_28+140delinsGTTT
ENST00000568219.5:c.2228+137_2228+140delinsGTTT	ENSP00000454703.2:n.2228+137_2228+140delinsGTTT
NM_024675.3:c.3113+137_3113+140delinsGTTT , LRG_308t1:c.3113+137_3113+140delinsGTTT	NP_078951.2:n.3113+137_3113+140delinsGTTT
XM_011545946.1:c.3119+137_3119+140delinsGTTT	XP_011544248.1:n.3119+137_3119+140delinsGTTT
XM_011545947.1:c.3119+137_3119+140delinsGTTT	XP_011544249.1:n.3119+137_3119+140delinsGTTT
XM_011545948.1:c.2228+137_2228+140delinsGTTT	XP_011544250.1:n.2228+137_2228+140delinsGTTT
XR_950851.1:n.3909+137_3909+140delinsGTTT
XM_011545946.2:c.3119+137_3119+140delinsGTTT	XP_011544248.1:n.3119+137_3119+140delinsGTTT
XM_011545947.2:c.3119+137_3119+140delinsGTTT	XP_011544249.1:n.3119+137_3119+140delinsGTTT
XM_011545948.2:c.2228+137_2228+140delinsGTTT	XP_011544250.1:n.2228+137_2228+140delinsGTTT
XM_017023671.1:c.3119+137_3119+140delinsGTTT	XP_016879160.1:n.3119+137_3119+140delinsGTTT
XM_017023672.2:c.3113+137_3113+140delinsGTTT	XP_016879161.1:n.3113+137_3113+140delinsGTTT
XM_017023673.2:c.3113+137_3113+140delinsGTTT	XP_016879162.1:n.3113+137_3113+140delinsGTTT
NM_024675.4:c.3113+137_3113+140delinsGTTT MANE Select	NP_078951.2:n.3113+137_3113+140delinsGTTT