Canonical Allele Identifier: CA1132973805
Gene: CACNA1F HGNC NCBI

Linked Data

dbSNP Id: rs2065714485

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49216273del , CM000685.2:g.49216273del GRCh38
NC_000023.10:g.49072733del , CM000685.1:g.49072733del GRCh37
NC_000023.9:g.48959677del NCBI36
NG_009095.2:g.22095del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.3236+110del MANE Select ENSP00000321618.6:n.3236+110del
ENST00000323022.9:c.3236+110del ENSP00000321618.5:n.3236+110del
ENST00000376251.5:c.3074+110del ENSP00000365427.1:n.3074+110del
ENST00000376265.2:c.3269+110del ENSP00000365441.2:n.3269+110del
NM_001256789.2:c.3236+110del NP_001243718.1:n.3236+110del
NM_001256790.2:c.3074+110del NP_001243719.1:n.3074+110del
NM_005183.3:c.3269+110del NP_005174.2:n.3269+110del
XM_011543983.1:c.3074+110del XP_011542285.1:n.3074+110del
XM_011543983.2:c.3074+110del XP_011542285.1:n.3074+110del
XM_017029836.1:c.503+110del XP_016885325.1:n.503+110del
NM_001256789.3:c.3236+110del MANE Select NP_001243718.1:n.3236+110del
NM_001256790.3:c.3074+110del NP_001243719.1:n.3074+110del
NM_005183.4:c.3269+110del NP_005174.2:n.3269+110del