Canonical Allele Identifier: CA2428540416
Gene: CACNA1F HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49218606T= , CM000685.2:g.49218606T= GRCh38
NC_000023.10:g.49075065T= , CM000685.1:g.49075065T= GRCh37
NC_000023.9:g.48962009T= NCBI36
NG_009095.2:g.19761A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.2840+23A= MANE Select ENSP00000321618.6:n.2840+23A=
ENST00000323022.9:c.2840+23A= ENSP00000321618.5:n.2840+23A=
ENST00000376251.5:c.2678+23A= ENSP00000365427.1:n.2678+23A=
ENST00000376265.2:c.2873+23A= ENSP00000365441.2:n.2873+23A=
NM_001256789.2:c.2840+23A= NP_001243718.1:n.2840+23A=
NM_001256790.2:c.2678+23A= NP_001243719.1:n.2678+23A=
NM_005183.3:c.2873+23A= NP_005174.2:n.2873+23A=
XM_011543983.1:c.2678+23A= XP_011542285.1:n.2678+23A=
XM_011543983.2:c.2678+23A= XP_011542285.1:n.2678+23A=
XM_017029836.1:c.107+23A= XP_016885325.1:n.107+23A=
NM_001256789.3:c.2840+23A= MANE Select NP_001243718.1:n.2840+23A=
NM_001256790.3:c.2678+23A= NP_001243719.1:n.2678+23A=
NM_005183.4:c.2873+23A= NP_005174.2:n.2873+23A=