Canonical Allele Identifier: CA516378328

Gene: CACNA1F

Linked Data

• MyVariant Identifiers: chrX:g.49079010T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49222551T>G , CM000685.2:g.49222551T>G	GRCh38
NC_000023.10:g.49079010T>G , CM000685.1:g.49079010T>G	GRCh37
NC_000023.9:g.48965954T>G	NCBI36
NG_009095.2:g.15816A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.2259A>C MANE Select	ENSP00000321618.6:p.Gly753=
ENST00000323022.9:c.2259A>C	ENSP00000321618.5:p.Gly753=
ENST00000376251.5:c.2097A>C	ENSP00000365427.1:p.Gly699=
ENST00000376265.2:c.2292A>C	ENSP00000365441.2:p.Gly764=
ENST00000480889.1:n.389A>C
NM_001256789.2:c.2259A>C	NP_001243718.1:p.Gly753=
NM_001256790.2:c.2097A>C	NP_001243719.1:p.Gly699=
NM_005183.3:c.2292A>C	NP_005174.2:p.Gly764=
XM_011543983.1:c.2097A>C	XP_011542285.1:p.Gly699=
XM_011543983.2:c.2097A>C	XP_011542285.1:p.Gly699=
NM_001256789.3:c.2259A>C MANE Select	NP_001243718.1:p.Gly753=
NM_001256790.3:c.2097A>C	NP_001243719.1:p.Gly699=
NM_005183.4:c.2292A>C	NP_005174.2:p.Gly764=