Canonical Allele Identifier: CA2213420968

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629228_23629230delinsGTT , CM000678.2:g.23629228_23629230delinsGTT	GRCh38
NC_000016.9:g.23640549_23640551delinsGTT , CM000678.1:g.23640549_23640551delinsGTT	GRCh37
NC_000016.8:g.23548050_23548052delinsGTT	NCBI36
NG_007406.1:g.17128_17130delinsAAC , LRG_308:g.17128_17130delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2566_2568delinsAAC	ENSP00000460666.3:p.Asn856=
ENST00000565038.2:c.*41_*43delinsAAC	ENSP00000459882.2:n.*41_*43delinsAAC
ENST00000566069.6:c.2560_2562delinsAAC	ENSP00000459237.2:p.Asn854=
ENST00000697377.2:c.2566_2568delinsAAC	ENSP00000513286.2:p.Asn856=
ENST00000697379.2:c.2566_2568delinsAAC	ENSP00000513287.2:p.Asn856=
ENST00000561514.2:c.1675_1677delinsAAC	ENSP00000460666.2:p.Asn559=
ENST00000697374.1:c.1675_1677delinsAAC	ENSP00000513284.1:p.Asn559=
ENST00000697375.1:n.3907_3909delinsAAC
ENST00000697376.1:c.1675_1677delinsAAC	ENSP00000513285.1:p.Asn559=
ENST00000697377.1:c.1675_1677delinsAAC	ENSP00000513286.1:p.Asn559=
ENST00000697378.1:n.3080_3082delinsAAC
ENST00000697379.1:c.1675_1677delinsAAC	ENSP00000513287.1:p.Asn559=
ENST00000697380.1:n.1852_1854delinsAAC
ENST00000697381.1:n.1255_1257delinsAAC
ENST00000697382.1:c.1675_1677delinsAAC	ENSP00000513288.1:p.Asn559=
ENST00000697383.1:c.94_96delinsAAC	ENSP00000513289.1:p.Asn32=
ENST00000697384.1:n.2714_2716delinsAAC
ENST00000261584.9:c.2560_2562delinsAAC MANE Select	ENSP00000261584.4:p.Asn854=
ENST00000261584.8:c.2560_2562delinsAAC	ENSP00000261584.4:p.Asn854=
ENST00000565038.1:c.132_134delinsAAC
ENST00000568219.5:c.1675_1677delinsAAC	ENSP00000454703.2:p.Asn559=
NM_024675.3:c.2560_2562delinsAAC , LRG_308t1:c.2560_2562delinsAAC	NP_078951.2:p.Asn854=
XM_011545946.1:c.2566_2568delinsAAC	XP_011544248.1:p.Asn856=
XM_011545947.1:c.2566_2568delinsAAC	XP_011544249.1:p.Asn856=
XM_011545948.1:c.1675_1677delinsAAC	XP_011544250.1:p.Asn559=
XR_950851.1:n.3356_3358delinsAAC
XM_011545946.2:c.2566_2568delinsAAC	XP_011544248.1:p.Asn856=
XM_011545947.2:c.2566_2568delinsAAC	XP_011544249.1:p.Asn856=
XM_011545948.2:c.1675_1677delinsAAC	XP_011544250.1:p.Asn559=
XM_017023671.1:c.2566_2568delinsAAC	XP_016879160.1:p.Asn856=
XM_017023672.2:c.2560_2562delinsAAC	XP_016879161.1:p.Asn854=
XM_017023673.2:c.2560_2562delinsAAC	XP_016879162.1:p.Asn854=
NM_024675.4:c.2560_2562delinsAAC MANE Select	NP_078951.2:p.Asn854=