Canonical Allele Identifier: CA2820835134

Gene: CACNA1F

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49216570_49216571insAGA , CM000685.2:g.49216570_49216571insAGA	GRCh38
NC_000023.10:g.49073030_49073031insAGA , CM000685.1:g.49073030_49073031insAGA	GRCh37
NC_000023.9:g.48959974_48959975insAGA	NCBI36
NG_009095.2:g.21796_21797insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.3090-43_3090-42insTCT MANE Select	ENSP00000321618.6:n.3090-43_3090-42insTCT
ENST00000323022.9:c.3090-43_3090-42insTCT	ENSP00000321618.5:n.3090-43_3090-42insTCT
ENST00000376251.5:c.2928-43_2928-42insTCT	ENSP00000365427.1:n.2928-43_2928-42insTCT
ENST00000376265.2:c.3123-43_3123-42insTCT	ENSP00000365441.2:n.3123-43_3123-42insTCT
NM_001256789.2:c.3090-43_3090-42insTCT	NP_001243718.1:n.3090-43_3090-42insTCT
NM_001256790.2:c.2928-43_2928-42insTCT	NP_001243719.1:n.2928-43_2928-42insTCT
NM_005183.3:c.3123-43_3123-42insTCT	NP_005174.2:n.3123-43_3123-42insTCT
XM_011543983.1:c.2928-43_2928-42insTCT	XP_011542285.1:n.2928-43_2928-42insTCT
XM_011543983.2:c.2928-43_2928-42insTCT	XP_011542285.1:n.2928-43_2928-42insTCT
XM_017029836.1:c.357-43_357-42insTCT	XP_016885325.1:n.357-43_357-42insTCT
NM_001256789.3:c.3090-43_3090-42insTCT MANE Select	NP_001243718.1:n.3090-43_3090-42insTCT
NM_001256790.3:c.2928-43_2928-42insTCT	NP_001243719.1:n.2928-43_2928-42insTCT
NM_005183.4:c.3123-43_3123-42insTCT	NP_005174.2:n.3123-43_3123-42insTCT