Canonical Allele Identifier: CA2213422881

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629948_23629949delinsCT , CM000678.2:g.23629948_23629949delinsCT	GRCh38
NC_000016.9:g.23641269_23641270delinsCT , CM000678.1:g.23641269_23641270delinsCT	GRCh37
NC_000016.8:g.23548770_23548771delinsCT	NCBI36
NG_007406.1:g.16409_16410delinsAG , LRG_308:g.16409_16410delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2211_2212delinsAG	ENSP00000460666.3:p.Pro737=
ENST00000565038.2:c.212-674_212-673delinsAG	ENSP00000459882.2:n.212-674_212-673delinsAG
ENST00000566069.6:c.2205_2206delinsAG	ENSP00000459237.2:p.Pro735=
ENST00000697377.2:c.2211_2212delinsAG	ENSP00000513286.2:p.Pro737=
ENST00000697379.2:c.2211_2212delinsAG	ENSP00000513287.2:p.Pro737=
ENST00000561514.2:c.1320_1321delinsAG	ENSP00000460666.2:p.Pro440=
ENST00000697374.1:c.1320_1321delinsAG	ENSP00000513284.1:p.Pro440=
ENST00000697375.1:n.3552_3553delinsAG
ENST00000697376.1:c.1320_1321delinsAG	ENSP00000513285.1:p.Pro440=
ENST00000697377.1:c.1320_1321delinsAG	ENSP00000513286.1:p.Pro440=
ENST00000697378.1:n.2725_2726delinsAG
ENST00000697379.1:c.1320_1321delinsAG	ENSP00000513287.1:p.Pro440=
ENST00000697380.1:n.1133_1134delinsAG
ENST00000697381.1:n.900_901delinsAG
ENST00000697382.1:c.1320_1321delinsAG	ENSP00000513288.1:p.Pro440=
ENST00000697383.1:c.49-674_49-673delinsAG	ENSP00000513289.1:n.49-674_49-673delinsAG
ENST00000697384.1:n.2359_2360delinsAG
ENST00000261584.9:c.2205_2206delinsAG MANE Select	ENSP00000261584.4:p.Pro735=
ENST00000261584.8:c.2205_2206delinsAG	ENSP00000261584.4:p.Pro735=
ENST00000565038.1:c.87-674_87-673delinsAG
ENST00000568219.5:c.1320_1321delinsAG	ENSP00000454703.2:p.Pro440=
NM_024675.3:c.2205_2206delinsAG , LRG_308t1:c.2205_2206delinsAG	NP_078951.2:p.Pro735=
XM_011545946.1:c.2211_2212delinsAG	XP_011544248.1:p.Pro737=
XM_011545947.1:c.2211_2212delinsAG	XP_011544249.1:p.Pro737=
XM_011545948.1:c.1320_1321delinsAG	XP_011544250.1:p.Pro440=
XR_950851.1:n.3001_3002delinsAG
XM_011545946.2:c.2211_2212delinsAG	XP_011544248.1:p.Pro737=
XM_011545947.2:c.2211_2212delinsAG	XP_011544249.1:p.Pro737=
XM_011545948.2:c.1320_1321delinsAG	XP_011544250.1:p.Pro440=
XM_017023671.1:c.2211_2212delinsAG	XP_016879160.1:p.Pro737=
XM_017023672.2:c.2205_2206delinsAG	XP_016879161.1:p.Pro735=
XM_017023673.2:c.2205_2206delinsAG	XP_016879162.1:p.Pro735=
NM_024675.4:c.2205_2206delinsAG MANE Select	NP_078951.2:p.Pro735=