Canonical Allele Identifier: CA2213412551

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623043_23623045delinsCTT , CM000678.2:g.23623043_23623045delinsCTT	GRCh38
NC_000016.9:g.23634364_23634366delinsCTT , CM000678.1:g.23634364_23634366delinsCTT	GRCh37
NC_000016.8:g.23541865_23541867delinsCTT	NCBI36
NG_007406.1:g.23313_23315delinsAAG , LRG_308:g.23313_23315delinsAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2926_2928delinsAAG	ENSP00000460666.3:p.Lys976=
ENST00000565038.2:c.*401_*403delinsAAG	ENSP00000459882.2:n.*401_*403delinsAAG
ENST00000566069.6:c.2920_2922delinsAAG	ENSP00000459237.2:p.Lys974=
ENST00000697377.2:c.2764_2766delinsAAG	ENSP00000513286.2:p.Lys922=
ENST00000697379.2:c.2926_2928delinsAAG	ENSP00000513287.2:p.Lys976=
ENST00000561514.2:c.2035_2037delinsAAG	ENSP00000460666.2:p.Lys679=
ENST00000697374.1:c.2035_2037delinsAAG	ENSP00000513284.1:p.Lys679=
ENST00000697375.1:n.4267_4269delinsAAG
ENST00000697376.1:c.2035_2037delinsAAG	ENSP00000513285.1:p.Lys679=
ENST00000697377.1:c.1873_1875delinsAAG	ENSP00000513286.1:p.Lys625=
ENST00000697378.1:n.3440_3442delinsAAG
ENST00000697379.1:c.2035_2037delinsAAG	ENSP00000513287.1:p.Lys679=
ENST00000697380.1:n.2212_2214delinsAAG
ENST00000697381.1:n.1615_1617delinsAAG
ENST00000697382.1:c.2035_2037delinsAAG	ENSP00000513288.1:p.Lys679=
ENST00000697383.1:c.454_456delinsAAG	ENSP00000513289.1:p.Lys152=
ENST00000261584.9:c.2920_2922delinsAAG MANE Select	ENSP00000261584.4:p.Lys974=
ENST00000261584.8:c.2920_2922delinsAAG	ENSP00000261584.4:p.Lys974=
ENST00000568219.5:c.2035_2037delinsAAG	ENSP00000454703.2:p.Lys679=
NM_024675.3:c.2920_2922delinsAAG , LRG_308t1:c.2920_2922delinsAAG	NP_078951.2:p.Lys974=
XM_011545946.1:c.2926_2928delinsAAG	XP_011544248.1:p.Lys976=
XM_011545947.1:c.2926_2928delinsAAG	XP_011544249.1:p.Lys976=
XM_011545948.1:c.2035_2037delinsAAG	XP_011544250.1:p.Lys679=
XR_950851.1:n.3716_3718delinsAAG
XM_011545946.2:c.2926_2928delinsAAG	XP_011544248.1:p.Lys976=
XM_011545947.2:c.2926_2928delinsAAG	XP_011544249.1:p.Lys976=
XM_011545948.2:c.2035_2037delinsAAG	XP_011544250.1:p.Lys679=
XM_017023671.1:c.2926_2928delinsAAG	XP_016879160.1:p.Lys976=
XM_017023672.2:c.2920_2922delinsAAG	XP_016879161.1:p.Lys974=
XM_017023673.2:c.2920_2922delinsAAG	XP_016879162.1:p.Lys974=
NM_024675.4:c.2920_2922delinsAAG MANE Select	NP_078951.2:p.Lys974=