Canonical Allele Identifier: CA2632327772

Gene: PALB2

Linked Data

• gnomAD v4: 16-23630582-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23630582T>A , CM000678.2:g.23630582T>A	GRCh38
NC_000016.9:g.23641903T>A , CM000678.1:g.23641903T>A	GRCh37
NC_000016.8:g.23549404T>A	NCBI36
NG_007406.1:g.15776A>T , LRG_308:g.15776A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.1691-113A>T	ENSP00000460666.3:n.1691-113A>T
ENST00000565038.2:c.212-1307A>T	ENSP00000459882.2:n.212-1307A>T
ENST00000566069.6:c.1685-113A>T	ENSP00000459237.2:n.1685-113A>T
ENST00000697377.2:c.1691-113A>T	ENSP00000513286.2:n.1691-113A>T
ENST00000697379.2:c.1691-113A>T	ENSP00000513287.2:n.1691-113A>T
ENST00000561514.2:c.800-113A>T	ENSP00000460666.2:n.800-113A>T
ENST00000697374.1:c.800-113A>T	ENSP00000513284.1:n.800-113A>T
ENST00000697375.1:n.3032-113A>T
ENST00000697376.1:c.800-113A>T	ENSP00000513285.1:n.800-113A>T
ENST00000697377.1:c.800-113A>T	ENSP00000513286.1:n.800-113A>T
ENST00000697378.1:n.2205-113A>T
ENST00000697379.1:c.800-113A>T	ENSP00000513287.1:n.800-113A>T
ENST00000697380.1:n.500A>T
ENST00000697381.1:n.380-113A>T
ENST00000697382.1:c.800-113A>T	ENSP00000513288.1:n.800-113A>T
ENST00000697383.1:c.49-1307A>T	ENSP00000513289.1:n.49-1307A>T
ENST00000697384.1:n.1839-113A>T
ENST00000261584.9:c.1685-113A>T MANE Select	ENSP00000261584.4:n.1685-113A>T
ENST00000261584.8:c.1685-113A>T	ENSP00000261584.4:n.1685-113A>T
ENST00000565038.1:c.87-1307A>T
ENST00000568219.5:c.800-113A>T	ENSP00000454703.2:n.800-113A>T
NM_024675.3:c.1685-113A>T , LRG_308t1:c.1685-113A>T	NP_078951.2:n.1685-113A>T
XM_011545946.1:c.1691-113A>T	XP_011544248.1:n.1691-113A>T
XM_011545947.1:c.1691-113A>T	XP_011544249.1:n.1691-113A>T
XM_011545948.1:c.800-113A>T	XP_011544250.1:n.800-113A>T
XR_950851.1:n.2481-113A>T
XM_011545946.2:c.1691-113A>T	XP_011544248.1:n.1691-113A>T
XM_011545947.2:c.1691-113A>T	XP_011544249.1:n.1691-113A>T
XM_011545948.2:c.800-113A>T	XP_011544250.1:n.800-113A>T
XM_017023671.1:c.1691-113A>T	XP_016879160.1:n.1691-113A>T
XM_017023672.2:c.1685-113A>T	XP_016879161.1:n.1685-113A>T
XM_017023673.2:c.1685-113A>T	XP_016879162.1:n.1685-113A>T
NM_024675.4:c.1685-113A>T MANE Select	NP_078951.2:n.1685-113A>T