Canonical Allele Identifier: CA2213413008

Gene: PALB2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23623127_23623128delinsTG , CM000678.2:g.23623127_23623128delinsTG	GRCh38
NC_000016.9:g.23634448_23634449delinsTG , CM000678.1:g.23634448_23634449delinsTG	GRCh37
NC_000016.8:g.23541949_23541950delinsTG	NCBI36
NG_007406.1:g.23230_23231delinsCA , LRG_308:g.23230_23231delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000561514.3:c.2843_2844delinsCA	ENSP00000460666.3:p.Ala948=
ENST00000565038.2:c.*318_*319delinsCA	ENSP00000459882.2:n.*318_*319delinsCA
ENST00000566069.6:c.2837_2838delinsCA	ENSP00000459237.2:p.Ala946=
ENST00000697377.2:c.2681_2682delinsCA	ENSP00000513286.2:p.Ala894=
ENST00000697379.2:c.2843_2844delinsCA	ENSP00000513287.2:p.Ala948=
ENST00000561514.2:c.1952_1953delinsCA	ENSP00000460666.2:p.Ala651=
ENST00000697374.1:c.1952_1953delinsCA	ENSP00000513284.1:p.Ala651=
ENST00000697375.1:n.4184_4185delinsCA
ENST00000697376.1:c.1952_1953delinsCA	ENSP00000513285.1:p.Ala651=
ENST00000697377.1:c.1790_1791delinsCA	ENSP00000513286.1:p.Ala597=
ENST00000697378.1:n.3357_3358delinsCA
ENST00000697379.1:c.1952_1953delinsCA	ENSP00000513287.1:p.Ala651=
ENST00000697380.1:n.2129_2130delinsCA
ENST00000697381.1:n.1532_1533delinsCA
ENST00000697382.1:c.1952_1953delinsCA	ENSP00000513288.1:p.Ala651=
ENST00000697383.1:c.371_372delinsCA	ENSP00000513289.1:p.Ala124=
ENST00000261584.9:c.2837_2838delinsCA MANE Select	ENSP00000261584.4:p.Ala946=
ENST00000261584.8:c.2837_2838delinsCA	ENSP00000261584.4:p.Ala946=
ENST00000568219.5:c.1952_1953delinsCA	ENSP00000454703.2:p.Ala651=
NM_024675.3:c.2837_2838delinsCA , LRG_308t1:c.2837_2838delinsCA	NP_078951.2:p.Ala946=
XM_011545946.1:c.2843_2844delinsCA	XP_011544248.1:p.Ala948=
XM_011545947.1:c.2843_2844delinsCA	XP_011544249.1:p.Ala948=
XM_011545948.1:c.1952_1953delinsCA	XP_011544250.1:p.Ala651=
XR_950851.1:n.3633_3634delinsCA
XM_011545946.2:c.2843_2844delinsCA	XP_011544248.1:p.Ala948=
XM_011545947.2:c.2843_2844delinsCA	XP_011544249.1:p.Ala948=
XM_011545948.2:c.1952_1953delinsCA	XP_011544250.1:p.Ala651=
XM_017023671.1:c.2843_2844delinsCA	XP_016879160.1:p.Ala948=
XM_017023672.2:c.2837_2838delinsCA	XP_016879161.1:p.Ala946=
XM_017023673.2:c.2837_2838delinsCA	XP_016879162.1:p.Ala946=
NM_024675.4:c.2837_2838delinsCA MANE Select	NP_078951.2:p.Ala946=