Canonical Allele Identifier: CA1955950849
Gene: CSRP3 HGNC NCBI

Linked Data

dbSNP Id: rs1850568560

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188613_19188620del , CM000673.2:g.19188613_19188620del GRCh38
NC_000011.9:g.19210160_19210167del , CM000673.1:g.19210160_19210167del GRCh37
NC_000011.8:g.19166736_19166743del NCBI36
NG_011932.2:g.26954_26961del , LRG_440:g.26954_26961del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.113-316_113-309del MANE Select ENSP00000265968.3:n.113-316_113-309del
ENST00000533783.2:c.113-316_113-309del ENSP00000431813.1:n.113-316_113-309del
ENST00000647990.1:c.113-316_113-309del ENSP00000496798.1:n.113-316_113-309del
ENST00000648719.1:c.113-3575_113-3568del ENSP00000497633.1:n.113-3575_113-3568del
ENST00000649235.1:c.113-316_113-309del ENSP00000497388.1:n.113-316_113-309del
ENST00000649842.1:c.113-2272_113-2265del ENSP00000497531.1:n.113-2272_113-2265del
ENST00000265968.7:c.113-316_113-309del ENSP00000265968.3:n.113-316_113-309del
ENST00000533783.1:c.113-316_113-309del ENSP00000431813.1:n.113-316_113-309del
NM_003476.4:c.113-316_113-309del NP_003467.1:n.113-316_113-309del
XM_024448698.1:c.113-2272_113-2265del XP_024304466.1:n.113-2272_113-2265del
NM_001369404.1:c.113-2272_113-2265del NP_001356333.1:n.113-2272_113-2265del
NM_003476.5:c.113-316_113-309del MANE Select NP_003467.1:n.113-316_113-309del