Canonical Allele Identifier: CA348182
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19185011C>T , CM000673.2:g.19185011C>T GRCh38
NC_000011.9:g.19206558C>T , CM000673.1:g.19206558C>T GRCh37
NC_000011.8:g.19163134C>T NCBI36
NG_011932.2:g.30563G>A , LRG_440:g.30563G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.449G>A MANE Select ENSP00000265968.3:p.Cys150Tyr
ENST00000533783.2:c.449G>A ENSP00000431813.1:p.Cys150Tyr
ENST00000647990.1:c.316G>A ENSP00000496798.1:p.Val106Met
ENST00000648719.1:c.147G>A ENSP00000497633.1:p.Leu49=
ENST00000649235.1:c.449G>A ENSP00000497388.1:p.Cys150Tyr
ENST00000649842.1:c.280G>A ENSP00000497531.1:p.Val94Met
ENST00000265968.7:c.449G>A ENSP00000265968.3:p.Cys150Tyr
ENST00000533783.1:c.449G>A ENSP00000431813.1:p.Cys150Tyr
NM_003476.4:c.449G>A NP_003467.1:p.Cys150Tyr
XM_024448698.1:c.280G>A XP_024304466.1:p.Val94Met
NM_001369404.1:c.280G>A NP_001356333.1:p.Val94Met
NM_003476.5:c.449G>A MANE Select NP_003467.1:p.Cys150Tyr