Canonical Allele Identifier: CA379887810
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19185045G>C , CM000673.2:g.19185045G>C GRCh38
NC_000011.9:g.19206592G>C , CM000673.1:g.19206592G>C GRCh37
NC_000011.8:g.19163168G>C NCBI36
NG_011932.2:g.30529C>G , LRG_440:g.30529C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.415C>G MANE Select ENSP00000265968.3:p.Pro139Ala
ENST00000533783.2:c.415C>G ENSP00000431813.1:p.Pro139Ala
ENST00000647990.1:c.282C>G ENSP00000496798.1:p.His94Gln
ENST00000648719.1:c.113C>G ENSP00000497633.1:p.Thr38Ser
ENST00000649235.1:c.415C>G ENSP00000497388.1:p.Pro139Ala
ENST00000649842.1:c.246C>G ENSP00000497531.1:p.Ser82Arg
ENST00000265968.7:c.415C>G ENSP00000265968.3:p.Pro139Ala
ENST00000533783.1:c.415C>G ENSP00000431813.1:p.Pro139Ala
NM_003476.4:c.415C>G NP_003467.1:p.Pro139Ala
XM_024448698.1:c.246C>G XP_024304466.1:p.Ser82Arg
NM_001369404.1:c.246C>G NP_001356333.1:p.Ser82Arg
NM_003476.5:c.415C>G MANE Select NP_003467.1:p.Pro139Ala