Canonical Allele Identifier: CA2213432575

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614088_23614089delinsAT , CM000678.2:g.23614088_23614089delinsAT	GRCh38
NC_000016.9:g.23625409_23625410delinsAT , CM000678.1:g.23625409_23625410delinsAT	GRCh37
NC_000016.8:g.23532910_23532911delinsAT	NCBI36
NG_007406.1:g.32269_32270delinsAT , LRG_308:g.32269_32270delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3122_3123delinsAT	ENSP00000460666.3:p.Asn1041=
ENST00000565038.2:c.*597_*598delinsAT	ENSP00000459882.2:n.*597_*598delinsAT
ENST00000566069.6:c.3116_3117delinsAT	ENSP00000459237.2:p.Asn1039=
ENST00000697377.2:c.2960_2961delinsAT	ENSP00000513286.2:p.Asn987=
ENST00000697379.2:c.3122_3123delinsAT	ENSP00000513287.2:p.Asn1041=
ENST00000561514.2:c.2231_2232delinsAT	ENSP00000460666.2:p.Asn744=
ENST00000697374.1:c.2231_2232delinsAT	ENSP00000513284.1:p.Asn744=
ENST00000697375.1:n.4463_4464delinsAT
ENST00000697376.1:c.2231_2232delinsAT	ENSP00000513285.1:p.Asn744=
ENST00000697377.1:c.2069_2070delinsAT	ENSP00000513286.1:p.Asn690=
ENST00000697378.1:n.3636_3637delinsAT
ENST00000697379.1:c.2231_2232delinsAT	ENSP00000513287.1:p.Asn744=
ENST00000697380.1:n.2406-6077_2406-6076delinsAT
ENST00000697381.1:n.1811_1812delinsAT
ENST00000697382.1:c.2229-6077_2229-6076delinsAT	ENSP00000513288.1:n.2229-6077_2229-6076delinsAT
ENST00000697383.1:c.650_651delinsAT	ENSP00000513289.1:p.Asn217=
ENST00000261584.9:c.3116_3117delinsAT MANE Select	ENSP00000261584.4:p.Asn1039=
ENST00000261584.8:c.3116_3117delinsAT	ENSP00000261584.4:p.Asn1039=
ENST00000566069.5:c.31_32delinsAT
ENST00000568219.5:c.2231_2232delinsAT	ENSP00000454703.2:p.Asn744=
NM_024675.3:c.3116_3117delinsAT , LRG_308t1:c.3116_3117delinsAT	NP_078951.2:p.Asn1039=
XM_011545946.1:c.3122_3123delinsAT	XP_011544248.1:p.Asn1041=
XM_011545947.1:c.3122_3123delinsAT	XP_011544249.1:p.Asn1041=
XM_011545948.1:c.2231_2232delinsAT	XP_011544250.1:p.Asn744=
XR_950851.1:n.3910-6077_3910-6076delinsAT
XM_011545946.2:c.3122_3123delinsAT	XP_011544248.1:p.Asn1041=
XM_011545947.2:c.3122_3123delinsAT	XP_011544249.1:p.Asn1041=
XM_011545948.2:c.2231_2232delinsAT	XP_011544250.1:p.Asn744=
XM_017023671.1:c.3119+7273_3119+7274delinsAT	XP_016879160.1:n.3119+7273_3119+7274delinsAT
XM_017023672.2:c.3113+7273_3113+7274delinsAT	XP_016879161.1:n.3113+7273_3113+7274delinsAT
XM_017023673.2:c.3116_3117delinsAT	XP_016879162.1:p.Asn1039=
NM_024675.4:c.3116_3117delinsAT MANE Select	NP_078951.2:p.Asn1039=