Canonical Allele Identifier: CA2428539694
Gene: CACNA1F HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49216354C= , CM000685.2:g.49216354C= GRCh38
NC_000023.10:g.49072814C= , CM000685.1:g.49072814C= GRCh37
NC_000023.9:g.48959758C= NCBI36
NG_009095.2:g.22013G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.3236+28G= MANE Select ENSP00000321618.6:n.3236+28G=
ENST00000323022.9:c.3236+28G= ENSP00000321618.5:n.3236+28G=
ENST00000376251.5:c.3074+28G= ENSP00000365427.1:n.3074+28G=
ENST00000376265.2:c.3269+28G= ENSP00000365441.2:n.3269+28G=
NM_001256789.2:c.3236+28G= NP_001243718.1:n.3236+28G=
NM_001256790.2:c.3074+28G= NP_001243719.1:n.3074+28G=
NM_005183.3:c.3269+28G= NP_005174.2:n.3269+28G=
XM_011543983.1:c.3074+28G= XP_011542285.1:n.3074+28G=
XM_011543983.2:c.3074+28G= XP_011542285.1:n.3074+28G=
XM_017029836.1:c.503+28G= XP_016885325.1:n.503+28G=
NM_001256789.3:c.3236+28G= MANE Select NP_001243718.1:n.3236+28G=
NM_001256790.3:c.3074+28G= NP_001243719.1:n.3074+28G=
NM_005183.4:c.3269+28G= NP_005174.2:n.3269+28G=