Canonical Allele Identifier: CA2579607659
Gene: CACNA1F HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49218425G>A , CM000685.2:g.49218425G>A GRCh38
NC_000023.10:g.49074884G>A , CM000685.1:g.49074884G>A GRCh37
NC_000023.9:g.48961828G>A NCBI36
NG_009095.2:g.19942C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000323022.10:c.2928+30C>T MANE Select ENSP00000321618.6:n.2928+30C>T
ENST00000323022.9:c.2928+30C>T ENSP00000321618.5:n.2928+30C>T
ENST00000376251.5:c.2766+30C>T ENSP00000365427.1:n.2766+30C>T
ENST00000376265.2:c.2961+30C>T ENSP00000365441.2:n.2961+30C>T
NM_001256789.2:c.2928+30C>T NP_001243718.1:n.2928+30C>T
NM_001256790.2:c.2766+30C>T NP_001243719.1:n.2766+30C>T
NM_005183.3:c.2961+30C>T NP_005174.2:n.2961+30C>T
XM_011543983.1:c.2766+30C>T XP_011542285.1:n.2766+30C>T
XM_011543983.2:c.2766+30C>T XP_011542285.1:n.2766+30C>T
XM_017029836.1:c.195+30C>T XP_016885325.1:n.195+30C>T
NM_001256789.3:c.2928+30C>T MANE Select NP_001243718.1:n.2928+30C>T
NM_001256790.3:c.2766+30C>T NP_001243719.1:n.2766+30C>T
NM_005183.4:c.2961+30C>T NP_005174.2:n.2961+30C>T