Canonical Allele Identifier: CA379888112
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188137G>C , CM000673.2:g.19188137G>C GRCh38
NC_000011.9:g.19209684G>C , CM000673.1:g.19209684G>C GRCh37
NC_000011.8:g.19166260G>C NCBI36
NG_011932.2:g.27437C>G , LRG_440:g.27437C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.280C>G MANE Select ENSP00000265968.3:p.Gln94Glu
ENST00000533783.2:c.280C>G ENSP00000431813.1:p.Gln94Glu
ENST00000647990.1:c.280C>G ENSP00000496798.1:p.His94Asp
ENST00000648719.1:c.113-3092C>G ENSP00000497633.1:n.113-3092C>G
ENST00000649235.1:c.280C>G ENSP00000497388.1:p.Gln94Glu
ENST00000649842.1:c.113-1789C>G ENSP00000497531.1:n.113-1789C>G
ENST00000265968.7:c.280C>G ENSP00000265968.3:p.Gln94Glu
ENST00000533783.1:c.280C>G ENSP00000431813.1:p.Gln94Glu
NM_003476.4:c.280C>G NP_003467.1:p.Gln94Glu
XM_024448698.1:c.113-1789C>G XP_024304466.1:n.113-1789C>G
NM_001369404.1:c.113-1789C>G NP_001356333.1:n.113-1789C>G
NM_003476.5:c.280C>G MANE Select NP_003467.1:p.Gln94Glu