Canonical Allele Identifier: CA2839076853

Gene: CACNA1F

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49218524dup , CM000685.2:g.49218524dup	GRCh38
NC_000023.10:g.49074983dup , CM000685.1:g.49074983dup	GRCh37
NC_000023.9:g.48961927dup	NCBI36
NG_009095.2:g.19844dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.2860dup MANE Select	ENSP00000321618.6:p.Val954GlyfsTer?
ENST00000323022.9:c.2860dup	ENSP00000321618.5:p.Val954GlyfsTer?
ENST00000376251.5:c.2698dup	ENSP00000365427.1:p.Val900GlyfsTer?
ENST00000376265.2:c.2893dup	ENSP00000365441.2:p.Val965GlyfsTer?
NM_001256789.2:c.2860dup	NP_001243718.1:p.Val954GlyfsTer?
NM_001256790.2:c.2698dup	NP_001243719.1:p.Val900GlyfsTer?
NM_005183.3:c.2893dup	NP_005174.2:p.Val965GlyfsTer?
XM_011543983.1:c.2698dup	XP_011542285.1:p.Val900GlyfsTer?
XM_011543983.2:c.2698dup	XP_011542285.1:p.Val900GlyfsTer?
XM_017029836.1:c.127dup	XP_016885325.1:p.Val43GlyfsTer?
NM_001256789.3:c.2860dup MANE Select	NP_001243718.1:p.Val954GlyfsTer?
NM_001256790.3:c.2698dup	NP_001243719.1:p.Val900GlyfsTer?
NM_005183.4:c.2893dup	NP_005174.2:p.Val965GlyfsTer?