Canonical Allele Identifier: CA2555394355
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188624_19188625insGGTGTG , CM000673.2:g.19188624_19188625insGGTGTG GRCh38
NC_000011.9:g.19210171_19210172insGGTGTG , CM000673.1:g.19210171_19210172insGGTGTG GRCh37
NC_000011.8:g.19166747_19166748insGGTGTG NCBI36
NG_011932.2:g.26954_26955insCCACAC , LRG_440:g.26954_26955insCCACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.113-316_113-315insCCACAC MANE Select ENSP00000265968.3:n.113-316_113-315insCCACAC
ENST00000533783.2:c.113-316_113-315insCCACAC ENSP00000431813.1:n.113-316_113-315insCCACAC
ENST00000647990.1:c.113-316_113-315insCCACAC ENSP00000496798.1:n.113-316_113-315insCCACAC
ENST00000648719.1:c.113-3575_113-3574insCCACAC ENSP00000497633.1:n.113-3575_113-3574insCCACAC
ENST00000649235.1:c.113-316_113-315insCCACAC ENSP00000497388.1:n.113-316_113-315insCCACAC
ENST00000649842.1:c.113-2272_113-2271insCCACAC ENSP00000497531.1:n.113-2272_113-2271insCCACAC
ENST00000265968.7:c.113-316_113-315insCCACAC ENSP00000265968.3:n.113-316_113-315insCCACAC
ENST00000533783.1:c.113-316_113-315insCCACAC ENSP00000431813.1:n.113-316_113-315insCCACAC
NM_003476.4:c.113-316_113-315insCCACAC NP_003467.1:n.113-316_113-315insCCACAC
XM_024448698.1:c.113-2272_113-2271insCCACAC XP_024304466.1:n.113-2272_113-2271insCCACAC
NM_001369404.1:c.113-2272_113-2271insCCACAC NP_001356333.1:n.113-2272_113-2271insCCACAC
NM_003476.5:c.113-316_113-315insCCACAC MANE Select NP_003467.1:n.113-316_113-315insCCACAC