Canonical Allele Identifier: CA2213420768

Gene: PALB2

Linked Data

• dbSNP Id: rs1966853246

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23629140_23629149del , CM000678.2:g.23629140_23629149del	GRCh38
NC_000016.9:g.23640461_23640470del , CM000678.1:g.23640461_23640470del	GRCh37
NC_000016.8:g.23547962_23547971del	NCBI36
NG_007406.1:g.17212_17221del , LRG_308:g.17212_17221del

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2592+58_2592+67del	ENSP00000460666.3:n.2592+58_2592+67del
ENST00000565038.2:c.*67+58_*67+67del	ENSP00000459882.2:n.*67+58_*67+67del
ENST00000566069.6:c.2586+58_2586+67del	ENSP00000459237.2:n.2586+58_2586+67del
ENST00000697377.2:c.2592+58_2592+67del	ENSP00000513286.2:n.2592+58_2592+67del
ENST00000697379.2:c.2592+58_2592+67del	ENSP00000513287.2:n.2592+58_2592+67del
ENST00000561514.2:c.1701+58_1701+67del	ENSP00000460666.2:n.1701+58_1701+67del
ENST00000697374.1:c.1701+58_1701+67del	ENSP00000513284.1:n.1701+58_1701+67del
ENST00000697375.1:n.3933+58_3933+67del
ENST00000697376.1:c.1701+58_1701+67del	ENSP00000513285.1:n.1701+58_1701+67del
ENST00000697377.1:c.1701+58_1701+67del	ENSP00000513286.1:n.1701+58_1701+67del
ENST00000697378.1:n.3106+58_3106+67del
ENST00000697379.1:c.1701+58_1701+67del	ENSP00000513287.1:n.1701+58_1701+67del
ENST00000697380.1:n.1878+58_1878+67del
ENST00000697381.1:n.1281+58_1281+67del
ENST00000697382.1:c.1701+58_1701+67del	ENSP00000513288.1:n.1701+58_1701+67del
ENST00000697383.1:c.120+58_120+67del	ENSP00000513289.1:n.120+58_120+67del
ENST00000697384.1:n.2798_2807del
ENST00000261584.9:c.2586+58_2586+67del MANE Select	ENSP00000261584.4:n.2586+58_2586+67del
ENST00000261584.8:c.2586+58_2586+67del	ENSP00000261584.4:n.2586+58_2586+67del
ENST00000565038.1:c.158+58_158+67del
ENST00000568219.5:c.1701+58_1701+67del	ENSP00000454703.2:n.1701+58_1701+67del
NM_024675.3:c.2586+58_2586+67del , LRG_308t1:c.2586+58_2586+67del	NP_078951.2:n.2586+58_2586+67del
XM_011545946.1:c.2592+58_2592+67del	XP_011544248.1:n.2592+58_2592+67del
XM_011545947.1:c.2592+58_2592+67del	XP_011544249.1:n.2592+58_2592+67del
XM_011545948.1:c.1701+58_1701+67del	XP_011544250.1:n.1701+58_1701+67del
XR_950851.1:n.3382+58_3382+67del
XM_011545946.2:c.2592+58_2592+67del	XP_011544248.1:n.2592+58_2592+67del
XM_011545947.2:c.2592+58_2592+67del	XP_011544249.1:n.2592+58_2592+67del
XM_011545948.2:c.1701+58_1701+67del	XP_011544250.1:n.1701+58_1701+67del
XM_017023671.1:c.2592+58_2592+67del	XP_016879160.1:n.2592+58_2592+67del
XM_017023672.2:c.2586+58_2586+67del	XP_016879161.1:n.2586+58_2586+67del
XM_017023673.2:c.2586+58_2586+67del	XP_016879162.1:n.2586+58_2586+67del
NM_024675.4:c.2586+58_2586+67del MANE Select	NP_078951.2:n.2586+58_2586+67del