Canonical Allele Identifier: CA2820835228
Gene: CACNA1F HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49216643_49216644insAG , CM000685.2:g.49216643_49216644insAG GRCh38
NC_000023.10:g.49073103_49073104insAG , CM000685.1:g.49073103_49073104insAG GRCh37
NC_000023.9:g.48960047_48960048insAG NCBI36
NG_009095.2:g.21723_21724insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.3090-116_3090-115insCT MANE Select ENSP00000321618.6:n.3090-116_3090-115insCT
ENST00000323022.9:c.3090-116_3090-115insCT ENSP00000321618.5:n.3090-116_3090-115insCT
ENST00000376251.5:c.2928-116_2928-115insCT ENSP00000365427.1:n.2928-116_2928-115insCT
ENST00000376265.2:c.3123-116_3123-115insCT ENSP00000365441.2:n.3123-116_3123-115insCT
NM_001256789.2:c.3090-116_3090-115insCT NP_001243718.1:n.3090-116_3090-115insCT
NM_001256790.2:c.2928-116_2928-115insCT NP_001243719.1:n.2928-116_2928-115insCT
NM_005183.3:c.3123-116_3123-115insCT NP_005174.2:n.3123-116_3123-115insCT
XM_011543983.1:c.2928-116_2928-115insCT XP_011542285.1:n.2928-116_2928-115insCT
XM_011543983.2:c.2928-116_2928-115insCT XP_011542285.1:n.2928-116_2928-115insCT
XM_017029836.1:c.357-116_357-115insCT XP_016885325.1:n.357-116_357-115insCT
NM_001256789.3:c.3090-116_3090-115insCT MANE Select NP_001243718.1:n.3090-116_3090-115insCT
NM_001256790.3:c.2928-116_2928-115insCT NP_001243719.1:n.2928-116_2928-115insCT
NM_005183.4:c.3123-116_3123-115insCT NP_005174.2:n.3123-116_3123-115insCT