Canonical Allele Identifier: CA13056178
Gene: PALM2AKAP2 HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.109834631G>A , CM000671.2:g.109834631G>A GRCh38
NC_000009.11:g.112596911G>A , CM000671.1:g.112596911G>A GRCh37
NC_000009.10:g.111636732G>A NCBI36
NG_054734.1:g.59335G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000374530.8:c.46-32860G>A MANE Select ENSP00000363654.3:n.46-32860G>A
ENST00000314527.9:c.46-32860G>A ENSP00000323805.4:n.46-32860G>A
ENST00000302798.7:c.46-32860G>A ENSP00000305861.7:n.46-32860G>A
ENST00000314527.8:c.46-32860G>A ENSP00000323805.4:n.46-32860G>A
ENST00000374530.7:c.46-32860G>A ENSP00000363654.3:n.46-32860G>A
ENST00000374531.6:c.52-32860G>A ENSP00000363656.2:n.52-32860G>A
ENST00000413420.5:c.46-32860G>A ENSP00000397839.1:n.46-32860G>A
ENST00000483909.5:c.46-32860G>A ENSP00000417525.1:n.46-32860G>A
NM_001037293.2:c.52-32860G>A NP_001032370.1:n.52-32860G>A
NM_007203.4:c.46-32860G>A NP_009134.1:n.46-32860G>A
NM_053016.5:c.46-32860G>A NP_443749.5:n.46-32860G>A
NM_147150.2:c.46-32860G>A NP_671492.1:n.46-32860G>A
NM_053016.6:c.46-32860G>A NP_443749.5:n.46-32860G>A
NM_007203.5:c.46-32860G>A MANE Select NP_009134.1:n.46-32860G>A
NM_147150.3:c.46-32860G>A NP_671492.1:n.46-32860G>A
NM_001037293.3:c.52-32860G>A NP_001032370.1:n.52-32860G>A