Canonical Allele Identifier: CA494177781

Gene: PALB2

Linked Data

• MyVariant Identifiers: chr16:g.23625409A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23614088A>G , CM000678.2:g.23614088A>G	GRCh38
NC_000016.9:g.23625409A>G , CM000678.1:g.23625409A>G	GRCh37
NC_000016.8:g.23532910A>G	NCBI36
NG_007406.1:g.32270T>C , LRG_308:g.32270T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000561514.3:c.3123T>C	ENSP00000460666.3:p.Asn1041=
ENST00000565038.2:c.*598T>C	ENSP00000459882.2:n.*598T>C
ENST00000566069.6:c.3117T>C	ENSP00000459237.2:p.Asn1039=
ENST00000697377.2:c.2961T>C	ENSP00000513286.2:p.Asn987=
ENST00000697379.2:c.3123T>C	ENSP00000513287.2:p.Asn1041=
ENST00000561514.2:c.2232T>C	ENSP00000460666.2:p.Asn744=
ENST00000697374.1:c.2232T>C	ENSP00000513284.1:p.Asn744=
ENST00000697375.1:n.4464T>C
ENST00000697376.1:c.2232T>C	ENSP00000513285.1:p.Asn744=
ENST00000697377.1:c.2070T>C	ENSP00000513286.1:p.Asn690=
ENST00000697378.1:n.3637T>C
ENST00000697379.1:c.2232T>C	ENSP00000513287.1:p.Asn744=
ENST00000697380.1:n.2406-6076T>C
ENST00000697381.1:n.1812T>C
ENST00000697382.1:c.2229-6076T>C	ENSP00000513288.1:n.2229-6076T>C
ENST00000697383.1:c.651T>C	ENSP00000513289.1:p.Asn217=
ENST00000261584.9:c.3117T>C MANE Select	ENSP00000261584.4:p.Asn1039=
ENST00000261584.8:c.3117T>C	ENSP00000261584.4:p.Asn1039=
ENST00000566069.5:c.32T>C
ENST00000568219.5:c.2232T>C	ENSP00000454703.2:p.Asn744=
NM_024675.3:c.3117T>C , LRG_308t1:c.3117T>C	NP_078951.2:p.Asn1039=
XM_011545946.1:c.3123T>C	XP_011544248.1:p.Asn1041=
XM_011545947.1:c.3123T>C	XP_011544249.1:p.Asn1041=
XM_011545948.1:c.2232T>C	XP_011544250.1:p.Asn744=
XR_950851.1:n.3910-6076T>C
XM_011545946.2:c.3123T>C	XP_011544248.1:p.Asn1041=
XM_011545947.2:c.3123T>C	XP_011544249.1:p.Asn1041=
XM_011545948.2:c.2232T>C	XP_011544250.1:p.Asn744=
XM_017023671.1:c.3119+7274T>C	XP_016879160.1:n.3119+7274T>C
XM_017023672.2:c.3113+7274T>C	XP_016879161.1:n.3113+7274T>C
XM_017023673.2:c.3117T>C	XP_016879162.1:p.Asn1039=
NM_024675.4:c.3117T>C MANE Select	NP_078951.2:p.Asn1039=