Canonical Allele Identifier: CA2790639596
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188618_19188619insGGTG , CM000673.2:g.19188618_19188619insGGTG GRCh38
NC_000011.9:g.19210165_19210166insGGTG , CM000673.1:g.19210165_19210166insGGTG GRCh37
NC_000011.8:g.19166741_19166742insGGTG NCBI36
NG_011932.2:g.26958_26959insCCAC , LRG_440:g.26958_26959insCCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.113-312_113-311insCCAC MANE Select ENSP00000265968.3:n.113-312_113-311insCCAC
ENST00000533783.2:c.113-312_113-311insCCAC ENSP00000431813.1:n.113-312_113-311insCCAC
ENST00000647990.1:c.113-312_113-311insCCAC ENSP00000496798.1:n.113-312_113-311insCCAC
ENST00000648719.1:c.113-3571_113-3570insCCAC ENSP00000497633.1:n.113-3571_113-3570insCCAC
ENST00000649235.1:c.113-312_113-311insCCAC ENSP00000497388.1:n.113-312_113-311insCCAC
ENST00000649842.1:c.113-2268_113-2267insCCAC ENSP00000497531.1:n.113-2268_113-2267insCCAC
ENST00000265968.7:c.113-312_113-311insCCAC ENSP00000265968.3:n.113-312_113-311insCCAC
ENST00000533783.1:c.113-312_113-311insCCAC ENSP00000431813.1:n.113-312_113-311insCCAC
NM_003476.4:c.113-312_113-311insCCAC NP_003467.1:n.113-312_113-311insCCAC
XM_024448698.1:c.113-2268_113-2267insCCAC XP_024304466.1:n.113-2268_113-2267insCCAC
NM_001369404.1:c.113-2268_113-2267insCCAC NP_001356333.1:n.113-2268_113-2267insCCAC
NM_003476.5:c.113-312_113-311insCCAC MANE Select NP_003467.1:n.113-312_113-311insCCAC