Canonical Allele Identifier: CA1132973925
Gene: CACNA1F HGNC NCBI

Linked Data

dbSNP Id: rs2065720134
gnomAD v3: X-49216623-G-T
gnomAD v4: X-49216623-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49216623G>T , CM000685.2:g.49216623G>T GRCh38
NC_000023.10:g.49073083G>T , CM000685.1:g.49073083G>T GRCh37
NC_000023.9:g.48960027G>T NCBI36
NG_009095.2:g.21744C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.3090-95C>A MANE Select ENSP00000321618.6:n.3090-95C>A
ENST00000323022.9:c.3090-95C>A ENSP00000321618.5:n.3090-95C>A
ENST00000376251.5:c.2928-95C>A ENSP00000365427.1:n.2928-95C>A
ENST00000376265.2:c.3123-95C>A ENSP00000365441.2:n.3123-95C>A
NM_001256789.2:c.3090-95C>A NP_001243718.1:n.3090-95C>A
NM_001256790.2:c.2928-95C>A NP_001243719.1:n.2928-95C>A
NM_005183.3:c.3123-95C>A NP_005174.2:n.3123-95C>A
XM_011543983.1:c.2928-95C>A XP_011542285.1:n.2928-95C>A
XM_011543983.2:c.2928-95C>A XP_011542285.1:n.2928-95C>A
XM_017029836.1:c.357-95C>A XP_016885325.1:n.357-95C>A
NM_001256789.3:c.3090-95C>A MANE Select NP_001243718.1:n.3090-95C>A
NM_001256790.3:c.2928-95C>A NP_001243719.1:n.2928-95C>A
NM_005183.4:c.3123-95C>A NP_005174.2:n.3123-95C>A