Canonical Allele Identifier: CA2820835202

Gene: CACNA1F

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49216628_49216629insAGA , CM000685.2:g.49216628_49216629insAGA	GRCh38
NC_000023.10:g.49073088_49073089insAGA , CM000685.1:g.49073088_49073089insAGA	GRCh37
NC_000023.9:g.48960032_48960033insAGA	NCBI36
NG_009095.2:g.21738_21739insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000323022.10:c.3090-101_3090-100insTCT MANE Select	ENSP00000321618.6:n.3090-101_3090-100insTCT
ENST00000323022.9:c.3090-101_3090-100insTCT	ENSP00000321618.5:n.3090-101_3090-100insTCT
ENST00000376251.5:c.2928-101_2928-100insTCT	ENSP00000365427.1:n.2928-101_2928-100insTCT
ENST00000376265.2:c.3123-101_3123-100insTCT	ENSP00000365441.2:n.3123-101_3123-100insTCT
NM_001256789.2:c.3090-101_3090-100insTCT	NP_001243718.1:n.3090-101_3090-100insTCT
NM_001256790.2:c.2928-101_2928-100insTCT	NP_001243719.1:n.2928-101_2928-100insTCT
NM_005183.3:c.3123-101_3123-100insTCT	NP_005174.2:n.3123-101_3123-100insTCT
XM_011543983.1:c.2928-101_2928-100insTCT	XP_011542285.1:n.2928-101_2928-100insTCT
XM_011543983.2:c.2928-101_2928-100insTCT	XP_011542285.1:n.2928-101_2928-100insTCT
XM_017029836.1:c.357-101_357-100insTCT	XP_016885325.1:n.357-101_357-100insTCT
NM_001256789.3:c.3090-101_3090-100insTCT MANE Select	NP_001243718.1:n.3090-101_3090-100insTCT
NM_001256790.3:c.2928-101_2928-100insTCT	NP_001243719.1:n.2928-101_2928-100insTCT
NM_005183.4:c.3123-101_3123-100insTCT	NP_005174.2:n.3123-101_3123-100insTCT