Canonical Allele Identifier: CA412964437
Gene: CACNA1F HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49217951C>T , CM000685.2:g.49217951C>T GRCh38
NC_000023.10:g.49074410C>T , CM000685.1:g.49074410C>T GRCh37
NC_000023.9:g.48961354C>T NCBI36
NG_009095.2:g.20416G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.2983G>A MANE Select ENSP00000321618.6:p.Val995Ile
ENST00000323022.9:c.2983G>A ENSP00000321618.5:p.Val995Ile
ENST00000376251.5:c.2821G>A ENSP00000365427.1:p.Val941Ile
ENST00000376265.2:c.3016G>A ENSP00000365441.2:p.Val1006Ile
NM_001256789.2:c.2983G>A NP_001243718.1:p.Val995Ile
NM_001256790.2:c.2821G>A NP_001243719.1:p.Val941Ile
NM_005183.3:c.3016G>A NP_005174.2:p.Val1006Ile
XM_011543983.1:c.2821G>A XP_011542285.1:p.Val941Ile
XM_011543983.2:c.2821G>A XP_011542285.1:p.Val941Ile
XM_017029836.1:c.250G>A XP_016885325.1:p.Val84Ile
NM_001256789.3:c.2983G>A MANE Select NP_001243718.1:p.Val995Ile
NM_001256790.3:c.2821G>A NP_001243719.1:p.Val941Ile
NM_005183.4:c.3016G>A NP_005174.2:p.Val1006Ile