Canonical Allele Identifier: CA2695222910

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614000_23614001insCA , CM000678.2:g.23614000_23614001insCA	GRCh38
NC_000016.9:g.23625321_23625322insCA , CM000678.1:g.23625321_23625322insCA	GRCh37
NC_000016.8:g.23532822_23532823insCA	NCBI36
NG_007406.1:g.32357_32358insTG , LRG_308:g.32357_32358insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3207+3_3207+4insTG	ENSP00000460666.3:n.3207+3_3207+4insTG
ENST00000565038.2:c.*682+3_*682+4insTG	ENSP00000459882.2:n.*682+3_*682+4insTG
ENST00000566069.6:c.3201+3_3201+4insTG	ENSP00000459237.2:n.3201+3_3201+4insTG
ENST00000697377.2:c.3045+3_3045+4insTG	ENSP00000513286.2:n.3045+3_3045+4insTG
ENST00000697379.2:c.3207+3_3207+4insTG	ENSP00000513287.2:n.3207+3_3207+4insTG
ENST00000561514.2:c.2316+3_2316+4insTG	ENSP00000460666.2:n.2316+3_2316+4insTG
ENST00000697374.1:c.2316+3_2316+4insTG	ENSP00000513284.1:n.2316+3_2316+4insTG
ENST00000697375.1:n.4548+3_4548+4insTG
ENST00000697376.1:c.2316+3_2316+4insTG	ENSP00000513285.1:n.2316+3_2316+4insTG
ENST00000697377.1:c.2154+3_2154+4insTG	ENSP00000513286.1:n.2154+3_2154+4insTG
ENST00000697378.1:n.3721+3_3721+4insTG
ENST00000697379.1:c.2316+3_2316+4insTG	ENSP00000513287.1:n.2316+3_2316+4insTG
ENST00000697380.1:n.2406-5989_2406-5988insTG
ENST00000697381.1:n.1896+3_1896+4insTG
ENST00000697382.1:c.2229-5989_2229-5988insTG	ENSP00000513288.1:n.2229-5989_2229-5988insTG
ENST00000697383.1:c.735+3_735+4insTG	ENSP00000513289.1:n.735+3_735+4insTG
ENST00000261584.9:c.3201+3_3201+4insTG MANE Select	ENSP00000261584.4:n.3201+3_3201+4insTG
ENST00000261584.8:c.3201+3_3201+4insTG	ENSP00000261584.4:n.3201+3_3201+4insTG
ENST00000566069.5:c.116+3_116+4insTG
ENST00000568219.5:c.2316+3_2316+4insTG	ENSP00000454703.2:n.2316+3_2316+4insTG
NM_024675.3:c.3201+3_3201+4insTG , LRG_308t1:c.3201+3_3201+4insTG	NP_078951.2:n.3201+3_3201+4insTG
XM_011545946.1:c.3207+3_3207+4insTG	XP_011544248.1:n.3207+3_3207+4insTG
XM_011545947.1:c.3207+3_3207+4insTG	XP_011544249.1:n.3207+3_3207+4insTG
XM_011545948.1:c.2316+3_2316+4insTG	XP_011544250.1:n.2316+3_2316+4insTG
XR_950851.1:n.3910-5989_3910-5988insTG
XM_011545946.2:c.3207+3_3207+4insTG	XP_011544248.1:n.3207+3_3207+4insTG
XM_011545947.2:c.3207+3_3207+4insTG	XP_011544249.1:n.3207+3_3207+4insTG
XM_011545948.2:c.2316+3_2316+4insTG	XP_011544250.1:n.2316+3_2316+4insTG
XM_017023671.1:c.3119+7361_3119+7362insTG	XP_016879160.1:n.3119+7361_3119+7362insTG
XM_017023672.2:c.3113+7361_3113+7362insTG	XP_016879161.1:n.3113+7361_3113+7362insTG
XM_017023673.2:c.3201+3_3201+4insTG	XP_016879162.1:n.3201+3_3201+4insTG
NM_024675.4:c.3201+3_3201+4insTG MANE Select	NP_078951.2:n.3201+3_3201+4insTG