Canonical Allele Identifier: CA2213409667

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23621366_23621369delinsTAAC , CM000678.2:g.23621366_23621369delinsTAAC	GRCh38
NC_000016.9:g.23632687_23632690delinsTAAC , CM000678.1:g.23632687_23632690delinsTAAC	GRCh37
NC_000016.8:g.23540188_23540191delinsTAAC	NCBI36
NG_007406.1:g.24989_24992delinsGTTA , LRG_308:g.24989_24992delinsGTTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.3112_3115delinsGTTA	ENSP00000460666.3:p.Val1038=
ENST00000565038.2:c.*587_*590delinsGTTA	ENSP00000459882.2:n.*587_*590delinsGTTA
ENST00000566069.6:c.3106_3109delinsGTTA	ENSP00000459237.2:p.Val1036=
ENST00000697377.2:c.2950_2953delinsGTTA	ENSP00000513286.2:p.Val984=
ENST00000697379.2:c.3112_3115delinsGTTA	ENSP00000513287.2:p.Val1038=
ENST00000561514.2:c.2221_2224delinsGTTA	ENSP00000460666.2:p.Val741=
ENST00000697374.1:c.2221_2224delinsGTTA	ENSP00000513284.1:p.Val741=
ENST00000697375.1:n.4453_4456delinsGTTA
ENST00000697376.1:c.2221_2224delinsGTTA	ENSP00000513285.1:p.Val741=
ENST00000697377.1:c.2059_2062delinsGTTA	ENSP00000513286.1:p.Val687=
ENST00000697378.1:n.3626_3629delinsGTTA
ENST00000697379.1:c.2221_2224delinsGTTA	ENSP00000513287.1:p.Val741=
ENST00000697380.1:n.2398_2401delinsGTTA
ENST00000697381.1:n.1801_1804delinsGTTA
ENST00000697382.1:c.2221_2224delinsGTTA	ENSP00000513288.1:p.Val741=
ENST00000697383.1:c.640_643delinsGTTA	ENSP00000513289.1:p.Val214=
ENST00000261584.9:c.3106_3109delinsGTTA MANE Select	ENSP00000261584.4:p.Val1036=
ENST00000261584.8:c.3106_3109delinsGTTA	ENSP00000261584.4:p.Val1036=
ENST00000566069.5:c.21_24delinsGTTA
ENST00000568219.5:c.2221_2224delinsGTTA	ENSP00000454703.2:p.Val741=
NM_024675.3:c.3106_3109delinsGTTA , LRG_308t1:c.3106_3109delinsGTTA	NP_078951.2:p.Val1036=
XM_011545946.1:c.3112_3115delinsGTTA	XP_011544248.1:p.Val1038=
XM_011545947.1:c.3112_3115delinsGTTA	XP_011544249.1:p.Val1038=
XM_011545948.1:c.2221_2224delinsGTTA	XP_011544250.1:p.Val741=
XR_950851.1:n.3902_3905delinsGTTA
XM_011545946.2:c.3112_3115delinsGTTA	XP_011544248.1:p.Val1038=
XM_011545947.2:c.3112_3115delinsGTTA	XP_011544249.1:p.Val1038=
XM_011545948.2:c.2221_2224delinsGTTA	XP_011544250.1:p.Val741=
XM_017023671.1:c.3112_3115delinsGTTA	XP_016879160.1:p.Val1038=
XM_017023672.2:c.3106_3109delinsGTTA	XP_016879161.1:p.Val1036=
XM_017023673.2:c.3106_3109delinsGTTA	XP_016879162.1:p.Val1036=
NM_024675.4:c.3106_3109delinsGTTA MANE Select	NP_078951.2:p.Val1036=