Canonical Allele Identifier: CA2213412530

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623040_23623042delinsCCT , CM000678.2:g.23623040_23623042delinsCCT	GRCh38
NC_000016.9:g.23634361_23634363delinsCCT , CM000678.1:g.23634361_23634363delinsCCT	GRCh37
NC_000016.8:g.23541862_23541864delinsCCT	NCBI36
NG_007406.1:g.23316_23318delinsAGG , LRG_308:g.23316_23318delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2929_2931delinsAGG	ENSP00000460666.3:p.Arg977=
ENST00000565038.2:c.*404_*406delinsAGG	ENSP00000459882.2:n.*404_*406delinsAGG
ENST00000566069.6:c.2923_2925delinsAGG	ENSP00000459237.2:p.Arg975=
ENST00000697377.2:c.2767_2769delinsAGG	ENSP00000513286.2:p.Arg923=
ENST00000697379.2:c.2929_2931delinsAGG	ENSP00000513287.2:p.Arg977=
ENST00000561514.2:c.2038_2040delinsAGG	ENSP00000460666.2:p.Arg680=
ENST00000697374.1:c.2038_2040delinsAGG	ENSP00000513284.1:p.Arg680=
ENST00000697375.1:n.4270_4272delinsAGG
ENST00000697376.1:c.2038_2040delinsAGG	ENSP00000513285.1:p.Arg680=
ENST00000697377.1:c.1876_1878delinsAGG	ENSP00000513286.1:p.Arg626=
ENST00000697378.1:n.3443_3445delinsAGG
ENST00000697379.1:c.2038_2040delinsAGG	ENSP00000513287.1:p.Arg680=
ENST00000697380.1:n.2215_2217delinsAGG
ENST00000697381.1:n.1618_1620delinsAGG
ENST00000697382.1:c.2038_2040delinsAGG	ENSP00000513288.1:p.Arg680=
ENST00000697383.1:c.457_459delinsAGG	ENSP00000513289.1:p.Arg153=
ENST00000261584.9:c.2923_2925delinsAGG MANE Select	ENSP00000261584.4:p.Arg975=
ENST00000261584.8:c.2923_2925delinsAGG	ENSP00000261584.4:p.Arg975=
ENST00000568219.5:c.2038_2040delinsAGG	ENSP00000454703.2:p.Arg680=
NM_024675.3:c.2923_2925delinsAGG , LRG_308t1:c.2923_2925delinsAGG	NP_078951.2:p.Arg975=
XM_011545946.1:c.2929_2931delinsAGG	XP_011544248.1:p.Arg977=
XM_011545947.1:c.2929_2931delinsAGG	XP_011544249.1:p.Arg977=
XM_011545948.1:c.2038_2040delinsAGG	XP_011544250.1:p.Arg680=
XR_950851.1:n.3719_3721delinsAGG
XM_011545946.2:c.2929_2931delinsAGG	XP_011544248.1:p.Arg977=
XM_011545947.2:c.2929_2931delinsAGG	XP_011544249.1:p.Arg977=
XM_011545948.2:c.2038_2040delinsAGG	XP_011544250.1:p.Arg680=
XM_017023671.1:c.2929_2931delinsAGG	XP_016879160.1:p.Arg977=
XM_017023672.2:c.2923_2925delinsAGG	XP_016879161.1:p.Arg975=
XM_017023673.2:c.2923_2925delinsAGG	XP_016879162.1:p.Arg975=
NM_024675.4:c.2923_2925delinsAGG MANE Select	NP_078951.2:p.Arg975=