Canonical Allele Identifier: CA2632329008

Gene: PALB2

Linked Data

• gnomAD v4: 16-23641273-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641273T>G , CM000678.2:g.23641273T>G	GRCh38
NC_000016.9:g.23652594T>G , CM000678.1:g.23652594T>G	GRCh37
NC_000016.8:g.23560095T>G	NCBI36
NG_007406.1:g.5085A>C , LRG_308:g.5085A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.-968A>C	ENSP00000460666.3:n.-968A>C
ENST00000566069.6:c.-116A>C	ENSP00000459237.2:n.-116A>C
ENST00000697377.2:c.-355A>C	ENSP00000513286.2:n.-355A>C
ENST00000697379.2:c.-261A>C	ENSP00000513287.2:n.-261A>C
ENST00000561514.2:c.-1859A>C	ENSP00000460666.2:n.-1859A>C
ENST00000697376.1:c.-1171A>C	ENSP00000513285.1:n.-1171A>C
ENST00000697377.1:c.-1246A>C	ENSP00000513286.1:n.-1246A>C
ENST00000697379.1:c.-1152A>C	ENSP00000513287.1:n.-1152A>C
ENST00000697382.1:c.-1910A>C	ENSP00000513288.1:n.-1910A>C
ENST00000697383.1:c.-116A>C	ENSP00000513289.1:n.-116A>C
ENST00000697384.1:n.39A>C
ENST00000261584.9:c.-116A>C MANE Select	ENSP00000261584.4:n.-116A>C
ENST00000261584.8:c.-116A>C	ENSP00000261584.4:n.-116A>C
ENST00000567003.1:n.29A>C
ENST00000568219.5:c.-984A>C	ENSP00000454703.2:n.-984A>C
NM_024675.3:c.-116A>C , LRG_308t1:c.-116A>C	NP_078951.2:n.-116A>C
XM_011545948.1:c.-1135A>C	XP_011544250.1:n.-1135A>C
XM_011545946.2:c.-968A>C	XP_011544248.1:n.-968A>C
XM_011545948.2:c.-1135A>C	XP_011544250.1:n.-1135A>C
XM_017023672.2:c.-116A>C	XP_016879161.1:n.-116A>C
XM_017023673.2:c.-116A>C	XP_016879162.1:n.-116A>C
NM_024675.4:c.-116A>C MANE Select	NP_078951.2:n.-116A>C