Canonical Allele Identifier: CA412964071
Gene: CACNA1F HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49216481A>T , CM000685.2:g.49216481A>T GRCh38
NC_000023.10:g.49072941A>T , CM000685.1:g.49072941A>T GRCh37
NC_000023.9:g.48959885A>T NCBI36
NG_009095.2:g.21886T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.3137T>A MANE Select ENSP00000321618.6:p.Val1046Asp
ENST00000323022.9:c.3137T>A ENSP00000321618.5:p.Val1046Asp
ENST00000376251.5:c.2975T>A ENSP00000365427.1:p.Val992Asp
ENST00000376265.2:c.3170T>A ENSP00000365441.2:p.Val1057Asp
NM_001256789.2:c.3137T>A NP_001243718.1:p.Val1046Asp
NM_001256790.2:c.2975T>A NP_001243719.1:p.Val992Asp
NM_005183.3:c.3170T>A NP_005174.2:p.Val1057Asp
XM_011543983.1:c.2975T>A XP_011542285.1:p.Val992Asp
XM_011543983.2:c.2975T>A XP_011542285.1:p.Val992Asp
XM_017029836.1:c.404T>A XP_016885325.1:p.Val135Asp
NM_001256789.3:c.3137T>A MANE Select NP_001243718.1:p.Val1046Asp
NM_001256790.3:c.2975T>A NP_001243719.1:p.Val992Asp
NM_005183.4:c.3170T>A NP_005174.2:p.Val1057Asp