Canonical Allele Identifier: CA2213432439
Gene: PALB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23613999_23614000delinsCT , CM000678.2:g.23613999_23614000delinsCT GRCh38
NC_000016.9:g.23625320_23625321delinsCT , CM000678.1:g.23625320_23625321delinsCT GRCh37
NC_000016.8:g.23532821_23532822delinsCT NCBI36
NG_007406.1:g.32358_32359delinsAG , LRG_308:g.32358_32359delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000561514.3:c.3207+4_3207+5delinsAG ENSP00000460666.3:n.3207+4_3207+5delinsAG...
ENST00000565038.2:c.*682+4_*682+5delinsAG ENSP00000459882.2:n.*682+4_*682+5delinsAG...
ENST00000566069.6:c.3201+4_3201+5delinsAG ENSP00000459237.2:n.3201+4_3201+5delinsAG...
ENST00000697377.2:c.3045+4_3045+5delinsAG ENSP00000513286.2:n.3045+4_3045+5delinsAG...
ENST00000697379.2:c.3207+4_3207+5delinsAG ENSP00000513287.2:n.3207+4_3207+5delinsAG...
ENST00000561514.2:c.2316+4_2316+5delinsAG ENSP00000460666.2:n.2316+4_2316+5delinsAG...
ENST00000697374.1:c.2316+4_2316+5delinsAG ENSP00000513284.1:n.2316+4_2316+5delinsAG...
ENST00000697375.1:n.4548+4_4548+5delinsAG
ENST00000697376.1:c.2316+4_2316+5delinsAG ENSP00000513285.1:n.2316+4_2316+5delinsAG...
ENST00000697377.1:c.2154+4_2154+5delinsAG ENSP00000513286.1:n.2154+4_2154+5delinsAG...
ENST00000697378.1:n.3721+4_3721+5delinsAG
ENST00000697379.1:c.2316+4_2316+5delinsAG ENSP00000513287.1:n.2316+4_2316+5delinsAG...
ENST00000697380.1:n.2406-5988_2406-5987delinsAG
ENST00000697381.1:n.1896+4_1896+5delinsAG
ENST00000697382.1:c.2229-5988_2229-5987delinsAG ENSP00000513288.1:n.2229-5988_2229-5987de...
ENST00000697383.1:c.735+4_735+5delinsAG ENSP00000513289.1:n.735+4_735+5delinsAG
ENST00000261584.9:c.3201+4_3201+5delinsAG MANE Select ENSP00000261584.4:n.3201+4_3201+5delinsAG...
ENST00000261584.8:c.3201+4_3201+5delinsAG ENSP00000261584.4:n.3201+4_3201+5delinsAG...
ENST00000566069.5:c.116+4_116+5delinsAG
ENST00000568219.5:c.2316+4_2316+5delinsAG ENSP00000454703.2:n.2316+4_2316+5delinsAG...
NM_024675.3:c.3201+4_3201+5delinsAG , LRG_308t1:c.3201+4_3201+5delinsAG NP_078951.2:n.3201+4_3201+5delinsAG
XM_011545946.1:c.3207+4_3207+5delinsAG XP_011544248.1:n.3207+4_3207+5delinsAG
XM_011545947.1:c.3207+4_3207+5delinsAG XP_011544249.1:n.3207+4_3207+5delinsAG
XM_011545948.1:c.2316+4_2316+5delinsAG XP_011544250.1:n.2316+4_2316+5delinsAG
XR_950851.1:n.3910-5988_3910-5987delinsAG
XM_011545946.2:c.3207+4_3207+5delinsAG XP_011544248.1:n.3207+4_3207+5delinsAG
XM_011545947.2:c.3207+4_3207+5delinsAG XP_011544249.1:n.3207+4_3207+5delinsAG
XM_011545948.2:c.2316+4_2316+5delinsAG XP_011544250.1:n.2316+4_2316+5delinsAG
XM_017023671.1:c.3119+7362_3119+7363delinsAG XP_016879160.1:n.3119+7362_3119+7363delin...
XM_017023672.2:c.3113+7362_3113+7363delinsAG XP_016879161.1:n.3113+7362_3113+7363delin...
XM_017023673.2:c.3201+4_3201+5delinsAG XP_016879162.1:n.3201+4_3201+5delinsAG
NM_024675.4:c.3201+4_3201+5delinsAG MANE Select NP_078951.2:n.3201+4_3201+5delinsAG