Canonical Allele Identifier: CA1955950626
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188200_19188201delinsAC , CM000673.2:g.19188200_19188201delinsAC GRCh38
NC_000011.9:g.19209747_19209748delinsAC , CM000673.1:g.19209747_19209748delinsAC GRCh37
NC_000011.8:g.19166323_19166324delinsAC NCBI36
NG_011932.2:g.27373_27374delinsGT , LRG_440:g.27373_27374delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.216_217delinsGT MANE Select ENSP00000265968.3:p.Gly72=
ENST00000533783.2:c.216_217delinsGT ENSP00000431813.1:p.Gly72=
ENST00000647990.1:c.216_217delinsGT ENSP00000496798.1:p.Gly72=
ENST00000648719.1:c.113-3156_113-3155delinsGT ENSP00000497633.1:n.113-3156_113-3155delinsGT
ENST00000649235.1:c.216_217delinsGT ENSP00000497388.1:p.Gly72=
ENST00000649842.1:c.113-1853_113-1852delinsGT ENSP00000497531.1:n.113-1853_113-1852delinsGT
ENST00000265968.7:c.216_217delinsGT ENSP00000265968.3:p.Gly72=
ENST00000533783.1:c.216_217delinsGT ENSP00000431813.1:p.Gly72=
NM_003476.4:c.216_217delinsGT NP_003467.1:p.Gly72=
XM_024448698.1:c.113-1853_113-1852delinsGT XP_024304466.1:n.113-1853_113-1852delinsGT
NM_001369404.1:c.113-1853_113-1852delinsGT NP_001356333.1:n.113-1853_113-1852delinsGT
NM_003476.5:c.216_217delinsGT MANE Select NP_003467.1:p.Gly72=