Canonical Allele Identifier: CA2213427779

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23634871_23634875delinsGAATA , CM000678.2:g.23634871_23634875delinsGAATA	GRCh38
NC_000016.9:g.23646192_23646196delinsGAATA , CM000678.1:g.23646192_23646196delinsGAATA	GRCh37
NC_000016.8:g.23553693_23553697delinsGAATA	NCBI36
NG_007406.1:g.11483_11487delinsTATTC , LRG_308:g.11483_11487delinsTATTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1677_1681delinsTATTC	ENSP00000460666.3:p.Phe559=
ENST00000565038.2:c.211+2975_211+2979delinsTATTC	ENSP00000459882.2:n.211+2975_211+2979delinsTATTC
ENST00000566069.6:c.1671_1675delinsTATTC	ENSP00000459237.2:p.Phe557=
ENST00000697377.2:c.1677_1681delinsTATTC	ENSP00000513286.2:p.Phe559=
ENST00000697379.2:c.1677_1681delinsTATTC	ENSP00000513287.2:p.Phe559=
ENST00000561514.2:c.786_790delinsTATTC	ENSP00000460666.2:p.Phe262=
ENST00000697374.1:c.786_790delinsTATTC	ENSP00000513284.1:p.Phe262=
ENST00000697375.1:n.3018_3022delinsTATTC
ENST00000697376.1:c.786_790delinsTATTC	ENSP00000513285.1:p.Phe262=
ENST00000697377.1:c.786_790delinsTATTC	ENSP00000513286.1:p.Phe262=
ENST00000697378.1:n.2191_2195delinsTATTC
ENST00000697379.1:c.786_790delinsTATTC	ENSP00000513287.1:p.Phe262=
ENST00000697382.1:c.786_790delinsTATTC	ENSP00000513288.1:p.Phe262=
ENST00000697383.1:c.49-5600_49-5596delinsTATTC	ENSP00000513289.1:n.49-5600_49-5596delinsTATTC
ENST00000697384.1:n.1825_1829delinsTATTC
ENST00000261584.9:c.1671_1675delinsTATTC MANE Select	ENSP00000261584.4:p.Phe557=
ENST00000261584.8:c.1671_1675delinsTATTC	ENSP00000261584.4:p.Phe557=
ENST00000565038.1:c.86+2975_86+2979delinsTATTC
ENST00000568219.5:c.786_790delinsTATTC	ENSP00000454703.2:p.Phe262=
NM_024675.3:c.1671_1675delinsTATTC , LRG_308t1:c.1671_1675delinsTATTC	NP_078951.2:p.Phe557=
XM_011545946.1:c.1677_1681delinsTATTC	XP_011544248.1:p.Phe559=
XM_011545947.1:c.1677_1681delinsTATTC	XP_011544249.1:p.Phe559=
XM_011545948.1:c.786_790delinsTATTC	XP_011544250.1:p.Phe262=
XR_950851.1:n.2467_2471delinsTATTC
XM_011545946.2:c.1677_1681delinsTATTC	XP_011544248.1:p.Phe559=
XM_011545947.2:c.1677_1681delinsTATTC	XP_011544249.1:p.Phe559=
XM_011545948.2:c.786_790delinsTATTC	XP_011544250.1:p.Phe262=
XM_017023671.1:c.1677_1681delinsTATTC	XP_016879160.1:p.Phe559=
XM_017023672.2:c.1671_1675delinsTATTC	XP_016879161.1:p.Phe557=
XM_017023673.2:c.1671_1675delinsTATTC	XP_016879162.1:p.Phe557=
NM_024675.4:c.1671_1675delinsTATTC MANE Select	NP_078951.2:p.Phe557=