Canonical Allele Identifier: CA2213436434

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641131_23641132delinsGA , CM000678.2:g.23641131_23641132delinsGA	GRCh38
NC_000016.9:g.23652452_23652453delinsGA , CM000678.1:g.23652452_23652453delinsGA	GRCh37
NC_000016.8:g.23559953_23559954delinsGA	NCBI36
NG_007406.1:g.5226_5227delinsTC , LRG_308:g.5226_5227delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-827_-826delinsTC	ENSP00000460666.3:n.-827_-826delinsTC
ENST00000565038.2:c.26_27delinsTC	ENSP00000459882.2:p.Leu9=
ENST00000566069.6:c.26_27delinsTC	ENSP00000459237.2:p.Leu9=
ENST00000697377.2:c.-214_-213delinsTC	ENSP00000513286.2:n.-214_-213delinsTC
ENST00000697379.2:c.-120_-119delinsTC	ENSP00000513287.2:n.-120_-119delinsTC
ENST00000561514.2:c.-1718_-1717delinsTC	ENSP00000460666.2:n.-1718_-1717delinsTC
ENST00000697374.1:c.-1309_-1308delinsTC	ENSP00000513284.1:n.-1309_-1308delinsTC
ENST00000697376.1:c.-1030_-1029delinsTC	ENSP00000513285.1:n.-1030_-1029delinsTC
ENST00000697377.1:c.-1105_-1104delinsTC	ENSP00000513286.1:n.-1105_-1104delinsTC
ENST00000697379.1:c.-1011_-1010delinsTC	ENSP00000513287.1:n.-1011_-1010delinsTC
ENST00000697382.1:c.-1769_-1768delinsTC	ENSP00000513288.1:n.-1769_-1768delinsTC
ENST00000697383.1:c.26_27delinsTC	ENSP00000513289.1:p.Leu9=
ENST00000697384.1:n.180_181delinsTC
ENST00000261584.9:c.26_27delinsTC MANE Select	ENSP00000261584.4:p.Leu9=
ENST00000261584.8:c.26_27delinsTC	ENSP00000261584.4:p.Leu9=
ENST00000567003.1:n.170_171delinsTC
ENST00000568219.5:c.-843_-842delinsTC	ENSP00000454703.2:n.-843_-842delinsTC
NM_024675.3:c.26_27delinsTC , LRG_308t1:c.26_27delinsTC	NP_078951.2:p.Leu9=
XM_011545948.1:c.-994_-993delinsTC	XP_011544250.1:n.-994_-993delinsTC
XM_011545946.2:c.-827_-826delinsTC	XP_011544248.1:n.-827_-826delinsTC
XM_011545947.2:c.-827_-826delinsTC	XP_011544249.1:n.-827_-826delinsTC
XM_011545948.2:c.-994_-993delinsTC	XP_011544250.1:n.-994_-993delinsTC
XM_017023671.1:c.-827_-826delinsTC	XP_016879160.1:n.-827_-826delinsTC
XM_017023672.2:c.26_27delinsTC	XP_016879161.1:p.Leu9=
XM_017023673.2:c.26_27delinsTC	XP_016879162.1:p.Leu9=
NM_024675.4:c.26_27delinsTC MANE Select	NP_078951.2:p.Leu9=