Canonical Allele Identifier: CA2213427653

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23634773_23634782delinsTAGAAAAGAA , CM000678.2:g.23634773_23634782delinsTAGAAAAGAA	GRCh38
NC_000016.9:g.23646094_23646103delinsTAGAAAAGAA , CM000678.1:g.23646094_23646103delinsTAGAAAAGAA	GRCh37
NC_000016.8:g.23553595_23553604delinsTAGAAAAGAA	NCBI36
NG_007406.1:g.11576_11585delinsTTCTTTTCTA , LRG_308:g.11576_11585delinsTTCTTTTCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.1690+80_1690+89delinsTTCTTTTCTA	ENSP00000460666.3:n.1690+80_1690+89delinsTTCTTTTCTA
ENST00000565038.2:c.211+3068_211+3077delinsTTCTTTTCTA	ENSP00000459882.2:n.211+3068_211+3077delinsTTCTTTTCTA
ENST00000566069.6:c.1684+80_1684+89delinsTTCTTTTCTA	ENSP00000459237.2:n.1684+80_1684+89delinsTTCTTTTCTA
ENST00000697377.2:c.1690+80_1690+89delinsTTCTTTTCTA	ENSP00000513286.2:n.1690+80_1690+89delinsTTCTTTTCTA
ENST00000697379.2:c.1690+80_1690+89delinsTTCTTTTCTA	ENSP00000513287.2:n.1690+80_1690+89delinsTTCTTTTCTA
ENST00000561514.2:c.799+80_799+89delinsTTCTTTTCTA	ENSP00000460666.2:n.799+80_799+89delinsTTCTTTTCTA
ENST00000697374.1:c.799+80_799+89delinsTTCTTTTCTA	ENSP00000513284.1:n.799+80_799+89delinsTTCTTTTCTA
ENST00000697375.1:n.3031+80_3031+89delinsTTCTTTTCTA
ENST00000697376.1:c.799+80_799+89delinsTTCTTTTCTA	ENSP00000513285.1:n.799+80_799+89delinsTTCTTTTCTA
ENST00000697377.1:c.799+80_799+89delinsTTCTTTTCTA	ENSP00000513286.1:n.799+80_799+89delinsTTCTTTTCTA
ENST00000697378.1:n.2204+80_2204+89delinsTTCTTTTCTA
ENST00000697379.1:c.799+80_799+89delinsTTCTTTTCTA	ENSP00000513287.1:n.799+80_799+89delinsTTCTTTTCTA
ENST00000697382.1:c.799+80_799+89delinsTTCTTTTCTA	ENSP00000513288.1:n.799+80_799+89delinsTTCTTTTCTA
ENST00000697383.1:c.49-5507_49-5498delinsTTCTTTTCTA	ENSP00000513289.1:n.49-5507_49-5498delinsTTCTTTTCTA
ENST00000697384.1:n.1838+80_1838+89delinsTTCTTTTCTA
ENST00000261584.9:c.1684+80_1684+89delinsTTCTTTTCTA MANE Select	ENSP00000261584.4:n.1684+80_1684+89delinsTTCTTTTCTA
ENST00000261584.8:c.1684+80_1684+89delinsTTCTTTTCTA	ENSP00000261584.4:n.1684+80_1684+89delinsTTCTTTTCTA
ENST00000565038.1:c.86+3068_86+3077delinsTTCTTTTCTA
ENST00000568219.5:c.799+80_799+89delinsTTCTTTTCTA	ENSP00000454703.2:n.799+80_799+89delinsTTCTTTTCTA
NM_024675.3:c.1684+80_1684+89delinsTTCTTTTCTA , LRG_308t1:c.1684+80_1684+89delinsTTCTTTTCTA	NP_078951.2:n.1684+80_1684+89delinsTTCTTTTCTA
XM_011545946.1:c.1690+80_1690+89delinsTTCTTTTCTA	XP_011544248.1:n.1690+80_1690+89delinsTTCTTTTCTA
XM_011545947.1:c.1690+80_1690+89delinsTTCTTTTCTA	XP_011544249.1:n.1690+80_1690+89delinsTTCTTTTCTA
XM_011545948.1:c.799+80_799+89delinsTTCTTTTCTA	XP_011544250.1:n.799+80_799+89delinsTTCTTTTCTA
XR_950851.1:n.2480+80_2480+89delinsTTCTTTTCTA
XM_011545946.2:c.1690+80_1690+89delinsTTCTTTTCTA	XP_011544248.1:n.1690+80_1690+89delinsTTCTTTTCTA
XM_011545947.2:c.1690+80_1690+89delinsTTCTTTTCTA	XP_011544249.1:n.1690+80_1690+89delinsTTCTTTTCTA
XM_011545948.2:c.799+80_799+89delinsTTCTTTTCTA	XP_011544250.1:n.799+80_799+89delinsTTCTTTTCTA
XM_017023671.1:c.1690+80_1690+89delinsTTCTTTTCTA	XP_016879160.1:n.1690+80_1690+89delinsTTCTTTTCTA
XM_017023672.2:c.1684+80_1684+89delinsTTCTTTTCTA	XP_016879161.1:n.1684+80_1684+89delinsTTCTTTTCTA
XM_017023673.2:c.1684+80_1684+89delinsTTCTTTTCTA	XP_016879162.1:n.1684+80_1684+89delinsTTCTTTTCTA
NM_024675.4:c.1684+80_1684+89delinsTTCTTTTCTA MANE Select	NP_078951.2:n.1684+80_1684+89delinsTTCTTTTCTA