Canonical Allele Identifier: CA10648165

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23641306C>T , CM000678.2:g.23641306C>T	GRCh38
NC_000016.9:g.23652627C>T , CM000678.1:g.23652627C>T	GRCh37
NC_000016.8:g.23560128C>T	NCBI36
NG_007406.1:g.5052G>A , LRG_308:g.5052G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697377.2:c.-388G>A	ENSP00000513286.2:n.-388G>A
ENST00000697379.2:c.-294G>A	ENSP00000513287.2:n.-294G>A
ENST00000697377.1:c.-1279G>A	ENSP00000513286.1:n.-1279G>A
ENST00000697379.1:c.-1185G>A	ENSP00000513287.1:n.-1185G>A
ENST00000697383.1:c.-149G>A	ENSP00000513289.1:n.-149G>A
ENST00000697384.1:n.6G>A
ENST00000261584.9:c.-149G>A MANE Select	ENSP00000261584.4:n.-149G>A
ENST00000261584.8:c.-149G>A	ENSP00000261584.4:n.-149G>A
NM_024675.3:c.-149G>A , LRG_308t1:c.-149G>A	NP_078951.2:n.-149G>A
XM_011545948.2:c.-1168G>A	XP_011544250.1:n.-1168G>A
XM_017023672.2:c.-149G>A	XP_016879161.1:n.-149G>A
XM_017023673.2:c.-149G>A	XP_016879162.1:n.-149G>A
NM_024675.4:c.-149G>A MANE Select	NP_078951.2:n.-149G>A