Canonical Allele Identifier: CA516377322

Gene: CACNA1F

Linked Data

• MyVariant Identifiers: chrX:g.49072931C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49216471C>T , CM000685.2:g.49216471C>T	GRCh38
NC_000023.10:g.49072931C>T , CM000685.1:g.49072931C>T	GRCh37
NC_000023.9:g.48959875C>T	NCBI36
NG_009095.2:g.21896G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.3147G>A MANE Select	ENSP00000321618.6:p.Arg1049=
ENST00000323022.9:c.3147G>A	ENSP00000321618.5:p.Arg1049=
ENST00000376251.5:c.2985G>A	ENSP00000365427.1:p.Arg995=
ENST00000376265.2:c.3180G>A	ENSP00000365441.2:p.Arg1060=
NM_001256789.2:c.3147G>A	NP_001243718.1:p.Arg1049=
NM_001256790.2:c.2985G>A	NP_001243719.1:p.Arg995=
NM_005183.3:c.3180G>A	NP_005174.2:p.Arg1060=
XM_011543983.1:c.2985G>A	XP_011542285.1:p.Arg995=
XM_011543983.2:c.2985G>A	XP_011542285.1:p.Arg995=
XM_017029836.1:c.414G>A	XP_016885325.1:p.Arg138=
NM_001256789.3:c.3147G>A MANE Select	NP_001243718.1:p.Arg1049=
NM_001256790.3:c.2985G>A	NP_001243719.1:p.Arg995=
NM_005183.4:c.3180G>A	NP_005174.2:p.Arg1060=