Canonical Allele Identifier: CA2632327800

Gene: PALB2

Linked Data

• gnomAD v4: 16-23630610-AATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630611_23630613del , CM000678.2:g.23630611_23630613del	GRCh38
NC_000016.9:g.23641932_23641934del , CM000678.1:g.23641932_23641934del	GRCh37
NC_000016.8:g.23549433_23549435del	NCBI36
NG_007406.1:g.15745_15747del , LRG_308:g.15745_15747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-144_1691-142del	ENSP00000460666.3:n.1691-144_1691-142del
ENST00000565038.2:c.212-1338_212-1336del	ENSP00000459882.2:n.212-1338_212-1336del
ENST00000566069.6:c.1685-144_1685-142del	ENSP00000459237.2:n.1685-144_1685-142del
ENST00000697377.2:c.1691-144_1691-142del	ENSP00000513286.2:n.1691-144_1691-142del
ENST00000697379.2:c.1691-144_1691-142del	ENSP00000513287.2:n.1691-144_1691-142del
ENST00000561514.2:c.800-144_800-142del	ENSP00000460666.2:n.800-144_800-142del
ENST00000697374.1:c.800-144_800-142del	ENSP00000513284.1:n.800-144_800-142del
ENST00000697375.1:n.3032-144_3032-142del
ENST00000697376.1:c.800-144_800-142del	ENSP00000513285.1:n.800-144_800-142del
ENST00000697377.1:c.800-144_800-142del	ENSP00000513286.1:n.800-144_800-142del
ENST00000697378.1:n.2205-144_2205-142del
ENST00000697379.1:c.800-144_800-142del	ENSP00000513287.1:n.800-144_800-142del
ENST00000697380.1:n.469_471del
ENST00000697381.1:n.379+106_379+108del
ENST00000697382.1:c.800-144_800-142del	ENSP00000513288.1:n.800-144_800-142del
ENST00000697383.1:c.49-1338_49-1336del	ENSP00000513289.1:n.49-1338_49-1336del
ENST00000697384.1:n.1839-144_1839-142del
ENST00000261584.9:c.1685-144_1685-142del MANE Select	ENSP00000261584.4:n.1685-144_1685-142del
ENST00000261584.8:c.1685-144_1685-142del	ENSP00000261584.4:n.1685-144_1685-142del
ENST00000565038.1:c.87-1338_87-1336del
ENST00000568219.5:c.800-144_800-142del	ENSP00000454703.2:n.800-144_800-142del
NM_024675.3:c.1685-144_1685-142del , LRG_308t1:c.1685-144_1685-142del	NP_078951.2:n.1685-144_1685-142del
XM_011545946.1:c.1691-144_1691-142del	XP_011544248.1:n.1691-144_1691-142del
XM_011545947.1:c.1691-144_1691-142del	XP_011544249.1:n.1691-144_1691-142del
XM_011545948.1:c.800-144_800-142del	XP_011544250.1:n.800-144_800-142del
XR_950851.1:n.2481-144_2481-142del
XM_011545946.2:c.1691-144_1691-142del	XP_011544248.1:n.1691-144_1691-142del
XM_011545947.2:c.1691-144_1691-142del	XP_011544249.1:n.1691-144_1691-142del
XM_011545948.2:c.800-144_800-142del	XP_011544250.1:n.800-144_800-142del
XM_017023671.1:c.1691-144_1691-142del	XP_016879160.1:n.1691-144_1691-142del
XM_017023672.2:c.1685-144_1685-142del	XP_016879161.1:n.1685-144_1685-142del
XM_017023673.2:c.1685-144_1685-142del	XP_016879162.1:n.1685-144_1685-142del
NM_024675.4:c.1685-144_1685-142del MANE Select	NP_078951.2:n.1685-144_1685-142del