Canonical Allele Identifier: CA379887522
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19182711C>T , CM000673.2:g.19182711C>T GRCh38
NC_000011.9:g.19204258C>T , CM000673.1:g.19204258C>T GRCh37
NC_000011.8:g.19160834C>T NCBI36
NG_011932.2:g.32863G>A , LRG_440:g.32863G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.544G>A MANE Select ENSP00000265968.3:p.Gly182Arg
ENST00000533783.2:c.544G>A ENSP00000431813.1:p.Gly182Arg
ENST00000647990.1:c.411G>A ENSP00000496798.1:p.Leu137=
ENST00000648719.1:c.*62G>A ENSP00000497633.1:n.*62G>A
ENST00000649235.1:c.544G>A ENSP00000497388.1:p.Gly182Arg
ENST00000649842.1:c.375G>A ENSP00000497531.1:p.Leu125=
ENST00000265968.7:c.544G>A ENSP00000265968.3:p.Gly182Arg
ENST00000533783.1:c.544G>A ENSP00000431813.1:p.Gly182Arg
NM_003476.4:c.544G>A NP_003467.1:p.Gly182Arg
XM_024448698.1:c.375G>A XP_024304466.1:p.Leu125=
NM_001369404.1:c.375G>A NP_001356333.1:p.Leu125=
NM_003476.5:c.544G>A MANE Select NP_003467.1:p.Gly182Arg