Canonical Allele Identifier: CA1152023442

Gene: CAMTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7663268_7663270delinsGCT , CM000663.2:g.7663268_7663270delinsGCT	GRCh38
NC_000001.10:g.7723328_7723330delinsGCT , CM000663.1:g.7723328_7723330delinsGCT	GRCh37
NC_000001.9:g.7645915_7645917delinsGCT	NCBI36
NG_053148.1:g.882945_882947delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476864.2:c.806-85_806-83delinsGCT	ENSP00000452319.2:n.806-85_806-83delinsGCT
ENST00000700414.1:c.*657-85_*657-83delinsGCT	ENSP00000514978.1:n.*657-85_*657-83delinsGCT
ENST00000700415.1:c.716-85_716-83delinsGCT	ENSP00000514979.1:n.716-85_716-83delinsGCT
ENST00000700417.1:c.734-85_734-83delinsGCT	ENSP00000514981.1:n.734-85_734-83delinsGCT
ENST00000700444.1:c.*575-85_*575-83delinsGCT	ENSP00000514992.1:n.*575-85_*575-83delinsGCT
ENST00000303635.12:c.806-85_806-83delinsGCT MANE Select	ENSP00000306522.6:n.806-85_806-83delinsGCT
ENST00000303635.11:c.806-85_806-83delinsGCT	ENSP00000306522.6:n.806-85_806-83delinsGCT
NM_015215.3:c.806-85_806-83delinsGCT	NP_056030.1:n.806-85_806-83delinsGCT
XM_011541083.1:c.806-85_806-83delinsGCT	XP_011539385.1:n.806-85_806-83delinsGCT
XM_011541084.1:c.806-85_806-83delinsGCT	XP_011539386.1:n.806-85_806-83delinsGCT
XM_011541085.1:c.794-85_794-83delinsGCT	XP_011539387.1:n.794-85_794-83delinsGCT
XM_011541086.1:c.806-85_806-83delinsGCT	XP_011539388.1:n.806-85_806-83delinsGCT
XM_011541087.1:c.734-85_734-83delinsGCT	XP_011539389.1:n.734-85_734-83delinsGCT
XM_011541088.1:c.716-85_716-83delinsGCT	XP_011539390.1:n.716-85_716-83delinsGCT
XM_011541089.1:c.806-85_806-83delinsGCT	XP_011539391.1:n.806-85_806-83delinsGCT
XM_011541090.1:c.806-85_806-83delinsGCT	XP_011539392.1:n.806-85_806-83delinsGCT
XM_011541091.1:c.806-85_806-83delinsGCT	XP_011539393.1:n.806-85_806-83delinsGCT
XM_011541092.1:c.806-85_806-83delinsGCT	XP_011539394.1:n.806-85_806-83delinsGCT
NM_001349608.1:c.716-85_716-83delinsGCT	NP_001336537.1:n.716-85_716-83delinsGCT
NM_001349609.1:c.806-85_806-83delinsGCT	NP_001336538.1:n.806-85_806-83delinsGCT
NM_001349610.1:c.806-85_806-83delinsGCT	NP_001336539.1:n.806-85_806-83delinsGCT
NM_001349612.1:c.716-85_716-83delinsGCT	NP_001336541.1:n.716-85_716-83delinsGCT
XM_011541083.2:c.806-85_806-83delinsGCT	XP_011539385.1:n.806-85_806-83delinsGCT
XM_011541084.2:c.806-85_806-83delinsGCT	XP_011539386.1:n.806-85_806-83delinsGCT
XM_011541086.3:c.806-85_806-83delinsGCT	XP_011539388.1:n.806-85_806-83delinsGCT
XM_011541087.2:c.734-85_734-83delinsGCT	XP_011539389.1:n.734-85_734-83delinsGCT
XM_011541088.2:c.716-85_716-83delinsGCT	XP_011539390.1:n.716-85_716-83delinsGCT
XM_011541090.3:c.806-85_806-83delinsGCT	XP_011539392.1:n.806-85_806-83delinsGCT
XM_011541091.2:c.806-85_806-83delinsGCT	XP_011539393.1:n.806-85_806-83delinsGCT
XM_011541092.3:c.806-85_806-83delinsGCT	XP_011539394.1:n.806-85_806-83delinsGCT
XM_017000774.2:c.806-85_806-83delinsGCT	XP_016856263.1:n.806-85_806-83delinsGCT
XM_017000777.1:c.806-85_806-83delinsGCT	XP_016856266.1:n.806-85_806-83delinsGCT
XM_017000778.1:c.806-85_806-83delinsGCT	XP_016856267.1:n.806-85_806-83delinsGCT
NM_015215.4:c.806-85_806-83delinsGCT MANE Select	NP_056030.1:n.806-85_806-83delinsGCT
NM_001349608.2:c.716-85_716-83delinsGCT	NP_001336537.1:n.716-85_716-83delinsGCT
NM_001349609.2:c.806-85_806-83delinsGCT	NP_001336538.1:n.806-85_806-83delinsGCT
NM_001349610.2:c.806-85_806-83delinsGCT	NP_001336539.1:n.806-85_806-83delinsGCT
NM_001349612.2:c.716-85_716-83delinsGCT	NP_001336541.1:n.716-85_716-83delinsGCT