Canonical Allele Identifier: CA2428539668
Gene: CACNA1F HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49216277G= , CM000685.2:g.49216277G= GRCh38
NC_000023.10:g.49072737G= , CM000685.1:g.49072737G= GRCh37
NC_000023.9:g.48959681G= NCBI36
NG_009095.2:g.22090C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.3236+105C= MANE Select ENSP00000321618.6:n.3236+105C=
ENST00000323022.9:c.3236+105C= ENSP00000321618.5:n.3236+105C=
ENST00000376251.5:c.3074+105C= ENSP00000365427.1:n.3074+105C=
ENST00000376265.2:c.3269+105C= ENSP00000365441.2:n.3269+105C=
NM_001256789.2:c.3236+105C= NP_001243718.1:n.3236+105C=
NM_001256790.2:c.3074+105C= NP_001243719.1:n.3074+105C=
NM_005183.3:c.3269+105C= NP_005174.2:n.3269+105C=
XM_011543983.1:c.3074+105C= XP_011542285.1:n.3074+105C=
XM_011543983.2:c.3074+105C= XP_011542285.1:n.3074+105C=
XM_017029836.1:c.503+105C= XP_016885325.1:n.503+105C=
NM_001256789.3:c.3236+105C= MANE Select NP_001243718.1:n.3236+105C=
NM_001256790.3:c.3074+105C= NP_001243719.1:n.3074+105C=
NM_005183.4:c.3269+105C= NP_005174.2:n.3269+105C=