Canonical Allele Identifier: CA2820835532
Gene: CACNA1F HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49218058_49218077del , CM000685.2:g.49218058_49218077del GRCh38
NC_000023.10:g.49074517_49074536del , CM000685.1:g.49074517_49074536del GRCh37
NC_000023.9:g.48961461_48961480del NCBI36
NG_009095.2:g.20297_20316del

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.2929-65_2929-46del MANE Select ENSP00000321618.6:n.2929-65_2929-46del
ENST00000323022.9:c.2929-65_2929-46del ENSP00000321618.5:n.2929-65_2929-46del
ENST00000376251.5:c.2767-65_2767-46del ENSP00000365427.1:n.2767-65_2767-46del
ENST00000376265.2:c.2962-65_2962-46del ENSP00000365441.2:n.2962-65_2962-46del
NM_001256789.2:c.2929-65_2929-46del NP_001243718.1:n.2929-65_2929-46del
NM_001256790.2:c.2767-65_2767-46del NP_001243719.1:n.2767-65_2767-46del
NM_005183.3:c.2962-65_2962-46del NP_005174.2:n.2962-65_2962-46del
XM_011543983.1:c.2767-65_2767-46del XP_011542285.1:n.2767-65_2767-46del
XM_011543983.2:c.2767-65_2767-46del XP_011542285.1:n.2767-65_2767-46del
XM_017029836.1:c.196-65_196-46del XP_016885325.1:n.196-65_196-46del
NM_001256789.3:c.2929-65_2929-46del MANE Select NP_001243718.1:n.2929-65_2929-46del
NM_001256790.3:c.2767-65_2767-46del NP_001243719.1:n.2767-65_2767-46del
NM_005183.4:c.2962-65_2962-46del NP_005174.2:n.2962-65_2962-46del