Canonical Allele Identifier: CA2790639593
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188615_19188621del , CM000673.2:g.19188615_19188621del GRCh38
NC_000011.9:g.19210162_19210168del , CM000673.1:g.19210162_19210168del GRCh37
NC_000011.8:g.19166738_19166744del NCBI36
NG_011932.2:g.26953_26959del , LRG_440:g.26953_26959del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.113-317_113-311del MANE Select ENSP00000265968.3:n.113-317_113-311del
ENST00000533783.2:c.113-317_113-311del ENSP00000431813.1:n.113-317_113-311del
ENST00000647990.1:c.113-317_113-311del ENSP00000496798.1:n.113-317_113-311del
ENST00000648719.1:c.113-3576_113-3570del ENSP00000497633.1:n.113-3576_113-3570del
ENST00000649235.1:c.113-317_113-311del ENSP00000497388.1:n.113-317_113-311del
ENST00000649842.1:c.113-2273_113-2267del ENSP00000497531.1:n.113-2273_113-2267del
ENST00000265968.7:c.113-317_113-311del ENSP00000265968.3:n.113-317_113-311del
ENST00000533783.1:c.113-317_113-311del ENSP00000431813.1:n.113-317_113-311del
NM_003476.4:c.113-317_113-311del NP_003467.1:n.113-317_113-311del
XM_024448698.1:c.113-2273_113-2267del XP_024304466.1:n.113-2273_113-2267del
NM_001369404.1:c.113-2273_113-2267del NP_001356333.1:n.113-2273_113-2267del
NM_003476.5:c.113-317_113-311del MANE Select NP_003467.1:n.113-317_113-311del