Canonical Allele Identifier: CA10409977
Community Standard Title: NM_001256789.3(CACNA1F):c.5446C>T (p.Arg1816Ter)
Gene: CACNA1F HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49206537G>A , CM000685.2:g.49206537G>A GRCh38
NC_000023.10:g.49062998G>A , CM000685.1:g.49062998G>A GRCh37
NC_000023.9:g.48949942G>A NCBI36
NG_009095.2:g.31830C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001256789.3:c.5446C>T MANE Select NP_001243718.1:p.Arg1816Ter
ENST00000323022.10:c.5446C>T MANE Select ENSP00000321618.6:p.Arg1816Ter
NM_001256789.2:c.5446C>T NP_001243718.1:p.Arg1816Ter
NM_001256790.2:c.5284C>T NP_001243719.1:p.Arg1762Ter
NM_001256790.3:c.5284C>T NP_001243719.1:p.Arg1762Ter
NM_005183.3:c.5479C>T NP_005174.2:p.Arg1827Ter
NM_005183.4:c.5479C>T NP_005174.2:p.Arg1827Ter
ENST00000323022.9:c.5446C>T ENSP00000321618.5:p.Arg1816Ter
ENST00000376251.5:c.5284C>T ENSP00000365427.1:p.Arg1762Ter
ENST00000376265.2:c.5479C>T ENSP00000365441.2:p.Arg1827Ter
XM_011543983.1:c.5263C>T XP_011542285.1:p.Arg1755Ter
XM_011543983.2:c.5263C>T XP_011542285.1:p.Arg1755Ter
XM_017029836.1:c.2629C>T XP_016885325.1:p.Arg877Ter