Canonical Allele Identifier: CA915951053

Gene: CACNA1F

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49211101C>T , CM000685.2:g.49211101C>T	GRCh38
NC_000023.10:g.49067561C>T , CM000685.1:g.49067561C>T	GRCh37
NC_000023.9:g.48954505C>T	NCBI36
NG_009095.2:g.27266G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001256789.3:c.4261-9G>A MANE Select	NP_001243718.1:n.4261-9G>A
ENST00000323022.10:c.4261-9G>A MANE Select	ENSP00000321618.6:n.4261-9G>A
NM_001256789.2:c.4261-9G>A	NP_001243718.1:n.4261-9G>A
NM_001256790.2:c.4099-9G>A	NP_001243719.1:n.4099-9G>A
NM_001256790.3:c.4099-9G>A	NP_001243719.1:n.4099-9G>A
NM_005183.3:c.4294-9G>A	NP_005174.2:n.4294-9G>A
NM_005183.4:c.4294-9G>A	NP_005174.2:n.4294-9G>A
ENST00000323022.9:c.4261-9G>A	ENSP00000321618.5:n.4261-9G>A
ENST00000376251.5:c.4099-9G>A	ENSP00000365427.1:n.4099-9G>A
ENST00000376265.2:c.4294-9G>A	ENSP00000365441.2:n.4294-9G>A
XM_011543983.1:c.4078-9G>A	XP_011542285.1:n.4078-9G>A
XM_011543983.2:c.4078-9G>A	XP_011542285.1:n.4078-9G>A
XM_017029836.1:c.1507-9G>A	XP_016885325.1:n.1507-9G>A