Canonical Allele Identifier: CA516377429

Gene: CACNA1F

Linked Data

• MyVariant Identifiers: chrX:g.49074405G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49217946G>C , CM000685.2:g.49217946G>C	GRCh38
NC_000023.10:g.49074405G>C , CM000685.1:g.49074405G>C	GRCh37
NC_000023.9:g.48961349G>C	NCBI36
NG_009095.2:g.20421C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.2988C>G MANE Select	ENSP00000321618.6:p.Thr996=
ENST00000323022.9:c.2988C>G	ENSP00000321618.5:p.Thr996=
ENST00000376251.5:c.2826C>G	ENSP00000365427.1:p.Thr942=
ENST00000376265.2:c.3021C>G	ENSP00000365441.2:p.Thr1007=
NM_001256789.2:c.2988C>G	NP_001243718.1:p.Thr996=
NM_001256790.2:c.2826C>G	NP_001243719.1:p.Thr942=
NM_005183.3:c.3021C>G	NP_005174.2:p.Thr1007=
XM_011543983.1:c.2826C>G	XP_011542285.1:p.Thr942=
XM_011543983.2:c.2826C>G	XP_011542285.1:p.Thr942=
XM_017029836.1:c.255C>G	XP_016885325.1:p.Thr85=
NM_001256789.3:c.2988C>G MANE Select	NP_001243718.1:p.Thr996=
NM_001256790.3:c.2826C>G	NP_001243719.1:p.Thr942=
NM_005183.4:c.3021C>G	NP_005174.2:p.Thr1007=