Canonical Allele Identifier: CA10583349
Gene: PALB2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.23603600C>T , CM000678.2:g.23603600C>T GRCh38
NC_000016.9:g.23614921C>T , CM000678.1:g.23614921C>T GRCh37
NC_000016.8:g.23522422C>T NCBI36
NG_007406.1:g.42758G>A , LRG_308:g.42758G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000561514.3:c.3426G>A ENSP00000460666.3:p.Trp1142Ter
ENST00000565038.2:c.*905G>A ENSP00000459882.2:n.*905G>A
ENST00000566069.6:c.*55G>A ENSP00000459237.2:n.*55G>A
ENST00000697377.2:c.3264G>A ENSP00000513286.2:p.Trp1088Ter
ENST00000697379.2:c.3426G>A ENSP00000513287.2:p.Trp1142Ter
ENST00000561514.2:c.2535G>A ENSP00000460666.2:p.Trp845Ter
ENST00000697374.1:c.2535G>A ENSP00000513284.1:p.Trp845Ter
ENST00000697375.1:n.4767G>A
ENST00000697376.1:c.*55G>A ENSP00000513285.1:n.*55G>A
ENST00000697377.1:c.2373G>A ENSP00000513286.1:p.Trp791Ter
ENST00000697378.1:n.3940G>A
ENST00000697379.1:c.2535G>A ENSP00000513287.1:p.Trp845Ter
ENST00000697380.1:n.2624G>A
ENST00000697381.1:n.2115G>A
ENST00000697382.1:c.*197G>A ENSP00000513288.1:n.*197G>A
ENST00000697383.1:c.954G>A ENSP00000513289.1:p.Trp318Ter
ENST00000261584.9:c.3420G>A MANE Select ENSP00000261584.4:p.Trp1140Ter
ENST00000261584.8:c.3420G>A ENSP00000261584.4:p.Trp1140Ter
ENST00000566069.5:c.186G>A
ENST00000568219.5:c.2535G>A ENSP00000454703.2:p.Trp845Ter
NM_024675.3:c.3420G>A , LRG_308t1:c.3420G>A NP_078951.2:p.Trp1140Ter
XM_011545946.1:c.3426G>A XP_011544248.1:p.Trp1142Ter
XM_011545947.1:c.*55G>A XP_011544249.1:n.*55G>A
XM_011545948.1:c.2535G>A XP_011544250.1:p.Trp845Ter
XR_950851.1:n.4128G>A
XM_011545946.2:c.3426G>A XP_011544248.1:p.Trp1142Ter
XM_011545947.2:c.*55G>A XP_011544249.1:n.*55G>A
XM_011545948.2:c.2535G>A XP_011544250.1:p.Trp845Ter
XM_017023671.1:c.3189G>A XP_016879160.1:p.Trp1063Ter
XM_017023672.2:c.3183G>A XP_016879161.1:p.Trp1061Ter
XM_017023673.2:c.*55G>A XP_016879162.1:n.*55G>A
NM_024675.4:c.3420G>A MANE Select NP_078951.2:p.Trp1140Ter
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