Canonical Allele Identifier: CA2790639611
Gene: CSRP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.19188621_19188625del , CM000673.2:g.19188621_19188625del GRCh38
NC_000011.9:g.19210168_19210172del , CM000673.1:g.19210168_19210172del GRCh37
NC_000011.8:g.19166744_19166748del NCBI36
NG_011932.2:g.26949_26953del , LRG_440:g.26949_26953del

Transcript Alleles

HGVS Amino-acid Change
ENST00000265968.9:c.113-321_113-317del MANE Select ENSP00000265968.3:n.113-321_113-317del
ENST00000533783.2:c.113-321_113-317del ENSP00000431813.1:n.113-321_113-317del
ENST00000647990.1:c.113-321_113-317del ENSP00000496798.1:n.113-321_113-317del
ENST00000648719.1:c.113-3580_113-3576del ENSP00000497633.1:n.113-3580_113-3576del
ENST00000649235.1:c.113-321_113-317del ENSP00000497388.1:n.113-321_113-317del
ENST00000649842.1:c.113-2277_113-2273del ENSP00000497531.1:n.113-2277_113-2273del
ENST00000265968.7:c.113-321_113-317del ENSP00000265968.3:n.113-321_113-317del
ENST00000533783.1:c.113-321_113-317del ENSP00000431813.1:n.113-321_113-317del
NM_003476.4:c.113-321_113-317del NP_003467.1:n.113-321_113-317del
XM_024448698.1:c.113-2277_113-2273del XP_024304466.1:n.113-2277_113-2273del
NM_001369404.1:c.113-2277_113-2273del NP_001356333.1:n.113-2277_113-2273del
NM_003476.5:c.113-321_113-317del MANE Select NP_003467.1:n.113-321_113-317del