Canonical Allele Identifier: CA2213424330

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630315_23630316delinsCT , CM000678.2:g.23630315_23630316delinsCT	GRCh38
NC_000016.9:g.23641636_23641637delinsCT , CM000678.1:g.23641636_23641637delinsCT	GRCh37
NC_000016.8:g.23549137_23549138delinsCT	NCBI36
NG_007406.1:g.16042_16043delinsAG , LRG_308:g.16042_16043delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1844_1845delinsAG	ENSP00000460666.3:p.Gln615=
ENST00000565038.2:c.212-1041_212-1040delinsAG	ENSP00000459882.2:n.212-1041_212-1040delinsAG
ENST00000566069.6:c.1838_1839delinsAG	ENSP00000459237.2:p.Gln613=
ENST00000697377.2:c.1844_1845delinsAG	ENSP00000513286.2:p.Gln615=
ENST00000697379.2:c.1844_1845delinsAG	ENSP00000513287.2:p.Gln615=
ENST00000561514.2:c.953_954delinsAG	ENSP00000460666.2:p.Gln318=
ENST00000697374.1:c.953_954delinsAG	ENSP00000513284.1:p.Gln318=
ENST00000697375.1:n.3185_3186delinsAG
ENST00000697376.1:c.953_954delinsAG	ENSP00000513285.1:p.Gln318=
ENST00000697377.1:c.953_954delinsAG	ENSP00000513286.1:p.Gln318=
ENST00000697378.1:n.2358_2359delinsAG
ENST00000697379.1:c.953_954delinsAG	ENSP00000513287.1:p.Gln318=
ENST00000697380.1:n.766_767delinsAG
ENST00000697381.1:n.533_534delinsAG
ENST00000697382.1:c.953_954delinsAG	ENSP00000513288.1:p.Gln318=
ENST00000697383.1:c.49-1041_49-1040delinsAG	ENSP00000513289.1:n.49-1041_49-1040delinsAG
ENST00000697384.1:n.1992_1993delinsAG
ENST00000261584.9:c.1838_1839delinsAG MANE Select	ENSP00000261584.4:p.Gln613=
ENST00000261584.8:c.1838_1839delinsAG	ENSP00000261584.4:p.Gln613=
ENST00000565038.1:c.87-1041_87-1040delinsAG
ENST00000568219.5:c.953_954delinsAG	ENSP00000454703.2:p.Gln318=
NM_024675.3:c.1838_1839delinsAG , LRG_308t1:c.1838_1839delinsAG	NP_078951.2:p.Gln613=
XM_011545946.1:c.1844_1845delinsAG	XP_011544248.1:p.Gln615=
XM_011545947.1:c.1844_1845delinsAG	XP_011544249.1:p.Gln615=
XM_011545948.1:c.953_954delinsAG	XP_011544250.1:p.Gln318=
XR_950851.1:n.2634_2635delinsAG
XM_011545946.2:c.1844_1845delinsAG	XP_011544248.1:p.Gln615=
XM_011545947.2:c.1844_1845delinsAG	XP_011544249.1:p.Gln615=
XM_011545948.2:c.953_954delinsAG	XP_011544250.1:p.Gln318=
XM_017023671.1:c.1844_1845delinsAG	XP_016879160.1:p.Gln615=
XM_017023672.2:c.1838_1839delinsAG	XP_016879161.1:p.Gln613=
XM_017023673.2:c.1838_1839delinsAG	XP_016879162.1:p.Gln613=
NM_024675.4:c.1838_1839delinsAG MANE Select	NP_078951.2:p.Gln613=