Canonical Allele Identifier: CA2693707025
Gene: CACNA1F HGNC NCBI

Linked Data

gnomAD v4: X-49216557-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.49216557T>C , CM000685.2:g.49216557T>C GRCh38
NC_000023.10:g.49073017T>C , CM000685.1:g.49073017T>C GRCh37
NC_000023.9:g.48959961T>C NCBI36
NG_009095.2:g.21810A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000323022.10:c.3090-29A>G MANE Select ENSP00000321618.6:n.3090-29A>G
ENST00000323022.9:c.3090-29A>G ENSP00000321618.5:n.3090-29A>G
ENST00000376251.5:c.2928-29A>G ENSP00000365427.1:n.2928-29A>G
ENST00000376265.2:c.3123-29A>G ENSP00000365441.2:n.3123-29A>G
NM_001256789.2:c.3090-29A>G NP_001243718.1:n.3090-29A>G
NM_001256790.2:c.2928-29A>G NP_001243719.1:n.2928-29A>G
NM_005183.3:c.3123-29A>G NP_005174.2:n.3123-29A>G
XM_011543983.1:c.2928-29A>G XP_011542285.1:n.2928-29A>G
XM_011543983.2:c.2928-29A>G XP_011542285.1:n.2928-29A>G
XM_017029836.1:c.357-29A>G XP_016885325.1:n.357-29A>G
NM_001256789.3:c.3090-29A>G MANE Select NP_001243718.1:n.3090-29A>G
NM_001256790.3:c.2928-29A>G NP_001243719.1:n.2928-29A>G
NM_005183.4:c.3123-29A>G NP_005174.2:n.3123-29A>G