Canonical Allele Identifier: CA719179043

Gene: PALB2

Linked Data

• dbSNP Id: rs775730652
• gnomAD v3: 16-23624232-CTT-C
• gnomAD v4: 16-23624232-CTT-C
• MyVariant Identifiers: chr16:g.23635554_23635555del (hg19) ; chr16:g.23624233_23624234del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23624236_23624237del , CM000678.2:g.23624236_23624237del	GRCh38
NC_000016.9:g.23635557_23635558del , CM000678.1:g.23635557_23635558del	GRCh37
NC_000016.8:g.23543058_23543059del	NCBI36
NG_007406.1:g.22124_22125del , LRG_308:g.22124_22125del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.2755-140_2755-139del	ENSP00000460666.3:n.2755-140_2755-139del
ENST00000565038.2:c.*230-140_*230-139del	ENSP00000459882.2:n.*230-140_*230-139del
ENST00000566069.6:c.2749-140_2749-139del	ENSP00000459237.2:n.2749-140_2749-139del
ENST00000697377.2:c.2593-140_2593-139del	ENSP00000513286.2:n.2593-140_2593-139del
ENST00000697379.2:c.2755-140_2755-139del	ENSP00000513287.2:n.2755-140_2755-139del
ENST00000561514.2:c.1864-140_1864-139del	ENSP00000460666.2:n.1864-140_1864-139del
ENST00000697374.1:c.1864-140_1864-139del	ENSP00000513284.1:n.1864-140_1864-139del
ENST00000697375.1:n.4096-140_4096-139del
ENST00000697376.1:c.1864-140_1864-139del	ENSP00000513285.1:n.1864-140_1864-139del
ENST00000697377.1:c.1702-140_1702-139del	ENSP00000513286.1:n.1702-140_1702-139del
ENST00000697378.1:n.3269-140_3269-139del
ENST00000697379.1:c.1864-140_1864-139del	ENSP00000513287.1:n.1864-140_1864-139del
ENST00000697380.1:n.2041-140_2041-139del
ENST00000697381.1:n.1444-140_1444-139del
ENST00000697382.1:c.1864-140_1864-139del	ENSP00000513288.1:n.1864-140_1864-139del
ENST00000697383.1:c.283-140_283-139del	ENSP00000513289.1:n.283-140_283-139del
ENST00000261584.9:c.2749-140_2749-139del MANE Select	ENSP00000261584.4:n.2749-140_2749-139del
ENST00000261584.8:c.2749-140_2749-139del	ENSP00000261584.4:n.2749-140_2749-139del
ENST00000565038.1:c.321-140_321-139del
ENST00000568219.5:c.1864-140_1864-139del	ENSP00000454703.2:n.1864-140_1864-139del
NM_024675.3:c.2749-140_2749-139del , LRG_308t1:c.2749-140_2749-139del	NP_078951.2:n.2749-140_2749-139del
XM_011545946.1:c.2755-140_2755-139del	XP_011544248.1:n.2755-140_2755-139del
XM_011545947.1:c.2755-140_2755-139del	XP_011544249.1:n.2755-140_2755-139del
XM_011545948.1:c.1864-140_1864-139del	XP_011544250.1:n.1864-140_1864-139del
XR_950851.1:n.3545-140_3545-139del
XM_011545946.2:c.2755-140_2755-139del	XP_011544248.1:n.2755-140_2755-139del
XM_011545947.2:c.2755-140_2755-139del	XP_011544249.1:n.2755-140_2755-139del
XM_011545948.2:c.1864-140_1864-139del	XP_011544250.1:n.1864-140_1864-139del
XM_017023671.1:c.2755-140_2755-139del	XP_016879160.1:n.2755-140_2755-139del
XM_017023672.2:c.2749-140_2749-139del	XP_016879161.1:n.2749-140_2749-139del
XM_017023673.2:c.2749-140_2749-139del	XP_016879162.1:n.2749-140_2749-139del
NM_024675.4:c.2749-140_2749-139del MANE Select	NP_078951.2:n.2749-140_2749-139del