Canonical Allele Identifier: CA10587718
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19182683del , CM000673.2:g.19182683del GRCh38
NC_000011.9:g.19204230del , CM000673.1:g.19204230del GRCh37
NC_000011.8:g.19160806del NCBI36
NG_011932.2:g.32894del , LRG_440:g.32894del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.575del MANE Select ENSP00000265968.3:p.Lys192ArgfsTer16
ENST00000533783.2:c.575del ENSP00000431813.1:p.Lys192ArgfsTer16
ENST00000647990.1:c.442del ENSP00000496798.1:p.Arg148GlufsTer21
ENST00000648719.1:c.*93del ENSP00000497633.1:n.*93del
ENST00000649235.1:c.575del ENSP00000497388.1:p.Lys192ArgfsTer16
ENST00000649842.1:c.406del ENSP00000497531.1:p.Arg136GlufsTer21
ENST00000265968.7:c.575del ENSP00000265968.3:p.Lys192ArgfsTer16
ENST00000533783.1:c.575del ENSP00000431813.1:p.Lys192ArgfsTer16
NM_003476.4:c.575del NP_003467.1:p.Lys192ArgfsTer16
XM_024448698.1:c.406del XP_024304466.1:p.Arg136GlufsTer21
NM_001369404.1:c.406del NP_001356333.1:p.Arg136GlufsTer21
NM_003476.5:c.575del MANE Select NP_003467.1:p.Lys192ArgfsTer16