Canonical Allele Identifier: CA379888093
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19186347A>C , CM000673.2:g.19186347A>C GRCh38
NC_000011.9:g.19207894A>C , CM000673.1:g.19207894A>C GRCh37
NC_000011.8:g.19164470A>C NCBI36
NG_011932.2:g.29227T>G , LRG_440:g.29227T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.283T>G MANE Select ENSP00000265968.3:p.Ser95Ala
ENST00000533783.2:c.283T>G ENSP00000431813.1:p.Ser95Ala
ENST00000647990.1:c.282-1302T>G ENSP00000496798.1:n.282-1302T>G
ENST00000648719.1:c.113-1302T>G ENSP00000497633.1:n.113-1302T>G
ENST00000649235.1:c.283T>G ENSP00000497388.1:p.Ser95Ala
ENST00000649842.1:c.114T>G ENSP00000497531.1:p.Ser38Arg
ENST00000265968.7:c.283T>G ENSP00000265968.3:p.Ser95Ala
ENST00000533783.1:c.283T>G ENSP00000431813.1:p.Ser95Ala
NM_003476.4:c.283T>G NP_003467.1:p.Ser95Ala
XM_024448698.1:c.114T>G XP_024304466.1:p.Ser38Arg
NM_001369404.1:c.114T>G NP_001356333.1:p.Ser38Arg
NM_003476.5:c.283T>G MANE Select NP_003467.1:p.Ser95Ala