Canonical Allele Identifier: CA5916535
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19184993G>A , CM000673.2:g.19184993G>A GRCh38
NC_000011.9:g.19206540G>A , CM000673.1:g.19206540G>A GRCh37
NC_000011.8:g.19163116G>A NCBI36
NG_011932.2:g.30581C>T , LRG_440:g.30581C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.467C>T MANE Select ENSP00000265968.3:p.Ser156Phe
ENST00000533783.2:c.467C>T ENSP00000431813.1:p.Ser156Phe
ENST00000647990.1:c.334C>T ENSP00000496798.1:p.Pro112Ser
ENST00000648719.1:c.165C>T ENSP00000497633.1:p.Val55=
ENST00000649235.1:c.467C>T ENSP00000497388.1:p.Ser156Phe
ENST00000649842.1:c.298C>T ENSP00000497531.1:p.Pro100Ser
ENST00000265968.7:c.467C>T ENSP00000265968.3:p.Ser156Phe
ENST00000533783.1:c.467C>T ENSP00000431813.1:p.Ser156Phe
NM_003476.4:c.467C>T NP_003467.1:p.Ser156Phe
XM_024448698.1:c.298C>T XP_024304466.1:p.Pro100Ser
NM_001369404.1:c.298C>T NP_001356333.1:p.Pro100Ser
NM_003476.5:c.467C>T MANE Select NP_003467.1:p.Ser156Phe