Canonical Allele Identifier: CA2213412462

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623026_23623027delinsCT , CM000678.2:g.23623026_23623027delinsCT	GRCh38
NC_000016.9:g.23634347_23634348delinsCT , CM000678.1:g.23634347_23634348delinsCT	GRCh37
NC_000016.8:g.23541848_23541849delinsCT	NCBI36
NG_007406.1:g.23331_23332delinsAG , LRG_308:g.23331_23332delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2944_2945delinsAG	ENSP00000460666.3:p.Ser982=
ENST00000565038.2:c.*419_*420delinsAG	ENSP00000459882.2:n.*419_*420delinsAG
ENST00000566069.6:c.2938_2939delinsAG	ENSP00000459237.2:p.Ser980=
ENST00000697377.2:c.2782_2783delinsAG	ENSP00000513286.2:p.Ser928=
ENST00000697379.2:c.2944_2945delinsAG	ENSP00000513287.2:p.Ser982=
ENST00000561514.2:c.2053_2054delinsAG	ENSP00000460666.2:p.Ser685=
ENST00000697374.1:c.2053_2054delinsAG	ENSP00000513284.1:p.Ser685=
ENST00000697375.1:n.4285_4286delinsAG
ENST00000697376.1:c.2053_2054delinsAG	ENSP00000513285.1:p.Ser685=
ENST00000697377.1:c.1891_1892delinsAG	ENSP00000513286.1:p.Ser631=
ENST00000697378.1:n.3458_3459delinsAG
ENST00000697379.1:c.2053_2054delinsAG	ENSP00000513287.1:p.Ser685=
ENST00000697380.1:n.2230_2231delinsAG
ENST00000697381.1:n.1633_1634delinsAG
ENST00000697382.1:c.2053_2054delinsAG	ENSP00000513288.1:p.Ser685=
ENST00000697383.1:c.472_473delinsAG	ENSP00000513289.1:p.Ser158=
ENST00000261584.9:c.2938_2939delinsAG MANE Select	ENSP00000261584.4:p.Ser980=
ENST00000261584.8:c.2938_2939delinsAG	ENSP00000261584.4:p.Ser980=
ENST00000568219.5:c.2053_2054delinsAG	ENSP00000454703.2:p.Ser685=
NM_024675.3:c.2938_2939delinsAG , LRG_308t1:c.2938_2939delinsAG	NP_078951.2:p.Ser980=
XM_011545946.1:c.2944_2945delinsAG	XP_011544248.1:p.Ser982=
XM_011545947.1:c.2944_2945delinsAG	XP_011544249.1:p.Ser982=
XM_011545948.1:c.2053_2054delinsAG	XP_011544250.1:p.Ser685=
XR_950851.1:n.3734_3735delinsAG
XM_011545946.2:c.2944_2945delinsAG	XP_011544248.1:p.Ser982=
XM_011545947.2:c.2944_2945delinsAG	XP_011544249.1:p.Ser982=
XM_011545948.2:c.2053_2054delinsAG	XP_011544250.1:p.Ser685=
XM_017023671.1:c.2944_2945delinsAG	XP_016879160.1:p.Ser982=
XM_017023672.2:c.2938_2939delinsAG	XP_016879161.1:p.Ser980=
XM_017023673.2:c.2938_2939delinsAG	XP_016879162.1:p.Ser980=
NM_024675.4:c.2938_2939delinsAG MANE Select	NP_078951.2:p.Ser980=