Canonical Allele Identifier: CA2213427696

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23635007_23635008delinsTG , CM000678.2:g.23635007_23635008delinsTG	GRCh38
NC_000016.9:g.23646328_23646329delinsTG , CM000678.1:g.23646328_23646329delinsTG	GRCh37
NC_000016.8:g.23553829_23553830delinsTG	NCBI36
NG_007406.1:g.11350_11351delinsCA , LRG_308:g.11350_11351delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1544_1545delinsCA	ENSP00000460666.3:p.Thr515=
ENST00000565038.2:c.211+2842_211+2843delinsCA	ENSP00000459882.2:n.211+2842_211+2843delinsCA
ENST00000566069.6:c.1538_1539delinsCA	ENSP00000459237.2:p.Thr513=
ENST00000697377.2:c.1544_1545delinsCA	ENSP00000513286.2:p.Thr515=
ENST00000697379.2:c.1544_1545delinsCA	ENSP00000513287.2:p.Thr515=
ENST00000561514.2:c.653_654delinsCA	ENSP00000460666.2:p.Thr218=
ENST00000697374.1:c.653_654delinsCA	ENSP00000513284.1:p.Thr218=
ENST00000697375.1:n.2885_2886delinsCA
ENST00000697376.1:c.653_654delinsCA	ENSP00000513285.1:p.Thr218=
ENST00000697377.1:c.653_654delinsCA	ENSP00000513286.1:p.Thr218=
ENST00000697378.1:n.2058_2059delinsCA
ENST00000697379.1:c.653_654delinsCA	ENSP00000513287.1:p.Thr218=
ENST00000697382.1:c.653_654delinsCA	ENSP00000513288.1:p.Thr218=
ENST00000697383.1:c.49-5733_49-5732delinsCA	ENSP00000513289.1:n.49-5733_49-5732delinsCA
ENST00000697384.1:n.1692_1693delinsCA
ENST00000261584.9:c.1538_1539delinsCA MANE Select	ENSP00000261584.4:p.Thr513=
ENST00000261584.8:c.1538_1539delinsCA	ENSP00000261584.4:p.Thr513=
ENST00000565038.1:c.86+2842_86+2843delinsCA
ENST00000568219.5:c.653_654delinsCA	ENSP00000454703.2:p.Thr218=
NM_024675.3:c.1538_1539delinsCA , LRG_308t1:c.1538_1539delinsCA	NP_078951.2:p.Thr513=
XM_011545946.1:c.1544_1545delinsCA	XP_011544248.1:p.Thr515=
XM_011545947.1:c.1544_1545delinsCA	XP_011544249.1:p.Thr515=
XM_011545948.1:c.653_654delinsCA	XP_011544250.1:p.Thr218=
XR_950851.1:n.2334_2335delinsCA
XM_011545946.2:c.1544_1545delinsCA	XP_011544248.1:p.Thr515=
XM_011545947.2:c.1544_1545delinsCA	XP_011544249.1:p.Thr515=
XM_011545948.2:c.653_654delinsCA	XP_011544250.1:p.Thr218=
XM_017023671.1:c.1544_1545delinsCA	XP_016879160.1:p.Thr515=
XM_017023672.2:c.1538_1539delinsCA	XP_016879161.1:p.Thr513=
XM_017023673.2:c.1538_1539delinsCA	XP_016879162.1:p.Thr513=
NM_024675.4:c.1538_1539delinsCA MANE Select	NP_078951.2:p.Thr513=