Canonical Allele Identifier: CA412909575

Gene: CACNA1F

Linked Data

• dbSNP Id: rs1182190028
• gnomAD v4: X-49222559-C-T
• MyVariant Identifiers: chrX:g.49079018C>T (hg19) ; chrX:g.49222559C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49222559C>T , CM000685.2:g.49222559C>T	GRCh38
NC_000023.10:g.49079018C>T , CM000685.1:g.49079018C>T	GRCh37
NC_000023.9:g.48965962C>T	NCBI36
NG_009095.2:g.15808G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.2251G>A MANE Select	ENSP00000321618.6:p.Ala751Thr
ENST00000323022.9:c.2251G>A	ENSP00000321618.5:p.Ala751Thr
ENST00000376251.5:c.2089G>A	ENSP00000365427.1:p.Ala697Thr
ENST00000376265.2:c.2284G>A	ENSP00000365441.2:p.Ala762Thr
ENST00000480889.1:n.381G>A
NM_001256789.2:c.2251G>A	NP_001243718.1:p.Ala751Thr
NM_001256790.2:c.2089G>A	NP_001243719.1:p.Ala697Thr
NM_005183.3:c.2284G>A	NP_005174.2:p.Ala762Thr
XM_011543983.1:c.2089G>A	XP_011542285.1:p.Ala697Thr
XM_011543983.2:c.2089G>A	XP_011542285.1:p.Ala697Thr
NM_001256789.3:c.2251G>A MANE Select	NP_001243718.1:p.Ala751Thr
NM_001256790.3:c.2089G>A	NP_001243719.1:p.Ala697Thr
NM_005183.4:c.2284G>A	NP_005174.2:p.Ala762Thr