Canonical Allele Identifier: CA2739290772

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623131_23623132delinsAA , CM000678.2:g.23623131_23623132delinsAA	GRCh38
NC_000016.9:g.23634452_23634453delinsAA , CM000678.1:g.23634452_23634453delinsAA	GRCh37
NC_000016.8:g.23541953_23541954delinsAA	NCBI36
NG_007406.1:g.23226_23227delinsTT , LRG_308:g.23226_23227delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2841-2_2841-1delinsTT	ENSP00000460666.3:n.2841-2_2841-1delinsTT
ENST00000565038.2:c.*316-2_*316-1delinsTT	ENSP00000459882.2:n.*316-2_*316-1delinsTT
ENST00000566069.6:c.2835-2_2835-1delinsTT	ENSP00000459237.2:n.2835-2_2835-1delinsTT
ENST00000697377.2:c.2679-2_2679-1delinsTT	ENSP00000513286.2:n.2679-2_2679-1delinsTT
ENST00000697379.2:c.2841-2_2841-1delinsTT	ENSP00000513287.2:n.2841-2_2841-1delinsTT
ENST00000561514.2:c.1950-2_1950-1delinsTT	ENSP00000460666.2:n.1950-2_1950-1delinsTT
ENST00000697374.1:c.1950-2_1950-1delinsTT	ENSP00000513284.1:n.1950-2_1950-1delinsTT
ENST00000697375.1:n.4182-2_4182-1delinsTT
ENST00000697376.1:c.1950-2_1950-1delinsTT	ENSP00000513285.1:n.1950-2_1950-1delinsTT
ENST00000697377.1:c.1788-2_1788-1delinsTT	ENSP00000513286.1:n.1788-2_1788-1delinsTT
ENST00000697378.1:n.3355-2_3355-1delinsTT
ENST00000697379.1:c.1950-2_1950-1delinsTT	ENSP00000513287.1:n.1950-2_1950-1delinsTT
ENST00000697380.1:n.2127-2_2127-1delinsTT
ENST00000697381.1:n.1530-2_1530-1delinsTT
ENST00000697382.1:c.1950-2_1950-1delinsTT	ENSP00000513288.1:n.1950-2_1950-1delinsTT
ENST00000697383.1:c.369-2_369-1delinsTT	ENSP00000513289.1:n.369-2_369-1delinsTT
ENST00000261584.9:c.2835-2_2835-1delinsTT MANE Select	ENSP00000261584.4:n.2835-2_2835-1delinsTT
ENST00000261584.8:c.2835-2_2835-1delinsTT	ENSP00000261584.4:n.2835-2_2835-1delinsTT
ENST00000568219.5:c.1950-2_1950-1delinsTT	ENSP00000454703.2:n.1950-2_1950-1delinsTT
NM_024675.3:c.2835-2_2835-1delinsTT , LRG_308t1:c.2835-2_2835-1delinsTT	NP_078951.2:n.2835-2_2835-1delinsTT
XM_011545946.1:c.2841-2_2841-1delinsTT	XP_011544248.1:n.2841-2_2841-1delinsTT
XM_011545947.1:c.2841-2_2841-1delinsTT	XP_011544249.1:n.2841-2_2841-1delinsTT
XM_011545948.1:c.1950-2_1950-1delinsTT	XP_011544250.1:n.1950-2_1950-1delinsTT
XR_950851.1:n.3631-2_3631-1delinsTT
XM_011545946.2:c.2841-2_2841-1delinsTT	XP_011544248.1:n.2841-2_2841-1delinsTT
XM_011545947.2:c.2841-2_2841-1delinsTT	XP_011544249.1:n.2841-2_2841-1delinsTT
XM_011545948.2:c.1950-2_1950-1delinsTT	XP_011544250.1:n.1950-2_1950-1delinsTT
XM_017023671.1:c.2841-2_2841-1delinsTT	XP_016879160.1:n.2841-2_2841-1delinsTT
XM_017023672.2:c.2835-2_2835-1delinsTT	XP_016879161.1:n.2835-2_2835-1delinsTT
XM_017023673.2:c.2835-2_2835-1delinsTT	XP_016879162.1:n.2835-2_2835-1delinsTT
NM_024675.4:c.2835-2_2835-1delinsTT MANE Select	NP_078951.2:n.2835-2_2835-1delinsTT