Canonical Allele Identifier: CA2632327757

Gene: PALB2

Linked Data

• gnomAD v4: 16-23630570-G-GTTTCTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630570_23630571insTTTCTTTT , CM000678.2:g.23630570_23630571insTTTCTTTT	GRCh38
NC_000016.9:g.23641891_23641892insTTTCTTTT , CM000678.1:g.23641891_23641892insTTTCTTTT	GRCh37
NC_000016.8:g.23549392_23549393insTTTCTTTT	NCBI36
NG_007406.1:g.15787_15788insAAAAGAAA , LRG_308:g.15787_15788insAAAAGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-102_1691-101insAAAAGAAA	ENSP00000460666.3:n.1691-102_1691-101insAAAAGAAA
ENST00000565038.2:c.212-1296_212-1295insAAAAGAAA	ENSP00000459882.2:n.212-1296_212-1295insAAAAGAAA
ENST00000566069.6:c.1685-102_1685-101insAAAAGAAA	ENSP00000459237.2:n.1685-102_1685-101insAAAAGAAA
ENST00000697377.2:c.1691-102_1691-101insAAAAGAAA	ENSP00000513286.2:n.1691-102_1691-101insAAAAGAAA
ENST00000697379.2:c.1691-102_1691-101insAAAAGAAA	ENSP00000513287.2:n.1691-102_1691-101insAAAAGAAA
ENST00000561514.2:c.800-102_800-101insAAAAGAAA	ENSP00000460666.2:n.800-102_800-101insAAAAGAAA
ENST00000697374.1:c.800-102_800-101insAAAAGAAA	ENSP00000513284.1:n.800-102_800-101insAAAAGAAA
ENST00000697375.1:n.3032-102_3032-101insAAAAGAAA
ENST00000697376.1:c.800-102_800-101insAAAAGAAA	ENSP00000513285.1:n.800-102_800-101insAAAAGAAA
ENST00000697377.1:c.800-102_800-101insAAAAGAAA	ENSP00000513286.1:n.800-102_800-101insAAAAGAAA
ENST00000697378.1:n.2205-102_2205-101insAAAAGAAA
ENST00000697379.1:c.800-102_800-101insAAAAGAAA	ENSP00000513287.1:n.800-102_800-101insAAAAGAAA
ENST00000697380.1:n.511_512insAAAAGAAA
ENST00000697381.1:n.380-102_380-101insAAAAGAAA
ENST00000697382.1:c.800-102_800-101insAAAAGAAA	ENSP00000513288.1:n.800-102_800-101insAAAAGAAA
ENST00000697383.1:c.49-1296_49-1295insAAAAGAAA	ENSP00000513289.1:n.49-1296_49-1295insAAAAGAAA
ENST00000697384.1:n.1839-102_1839-101insAAAAGAAA
ENST00000261584.9:c.1685-102_1685-101insAAAAGAAA MANE Select	ENSP00000261584.4:n.1685-102_1685-101insAAAAGAAA
ENST00000261584.8:c.1685-102_1685-101insAAAAGAAA	ENSP00000261584.4:n.1685-102_1685-101insAAAAGAAA
ENST00000565038.1:c.87-1296_87-1295insAAAAGAAA
ENST00000568219.5:c.800-102_800-101insAAAAGAAA	ENSP00000454703.2:n.800-102_800-101insAAAAGAAA
NM_024675.3:c.1685-102_1685-101insAAAAGAAA , LRG_308t1:c.1685-102_1685-101insAAAAGAAA	NP_078951.2:n.1685-102_1685-101insAAAAGAAA
XM_011545946.1:c.1691-102_1691-101insAAAAGAAA	XP_011544248.1:n.1691-102_1691-101insAAAAGAAA
XM_011545947.1:c.1691-102_1691-101insAAAAGAAA	XP_011544249.1:n.1691-102_1691-101insAAAAGAAA
XM_011545948.1:c.800-102_800-101insAAAAGAAA	XP_011544250.1:n.800-102_800-101insAAAAGAAA
XR_950851.1:n.2481-102_2481-101insAAAAGAAA
XM_011545946.2:c.1691-102_1691-101insAAAAGAAA	XP_011544248.1:n.1691-102_1691-101insAAAAGAAA
XM_011545947.2:c.1691-102_1691-101insAAAAGAAA	XP_011544249.1:n.1691-102_1691-101insAAAAGAAA
XM_011545948.2:c.800-102_800-101insAAAAGAAA	XP_011544250.1:n.800-102_800-101insAAAAGAAA
XM_017023671.1:c.1691-102_1691-101insAAAAGAAA	XP_016879160.1:n.1691-102_1691-101insAAAAGAAA
XM_017023672.2:c.1685-102_1685-101insAAAAGAAA	XP_016879161.1:n.1685-102_1685-101insAAAAGAAA
XM_017023673.2:c.1685-102_1685-101insAAAAGAAA	XP_016879162.1:n.1685-102_1685-101insAAAAGAAA
NM_024675.4:c.1685-102_1685-101insAAAAGAAA MANE Select	NP_078951.2:n.1685-102_1685-101insAAAAGAAA