Canonical Allele Identifier: CA1152023706

Gene: CAMTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7663706_7663716delinsGCCTCTGTGAT , CM000663.2:g.7663706_7663716delinsGCCTCTGTGAT	GRCh38
NC_000001.10:g.7723766_7723776delinsGCCTCTGTGAT , CM000663.1:g.7723766_7723776delinsGCCTCTGTGAT	GRCh37
NC_000001.9:g.7646353_7646363delinsGCCTCTGTGAT	NCBI36
NG_053148.1:g.883383_883393delinsGCCTCTGTGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476864.2:c.1159_1169delinsGCCTCTGTGAT	ENSP00000452319.2:p.Ala387=
ENST00000700414.1:c.*1010_*1020delinsGCCTCTGTGAT	ENSP00000514978.1:n.*1010_*1020delinsGCCTCTGTGAT
ENST00000700415.1:c.1069_1079delinsGCCTCTGTGAT	ENSP00000514979.1:p.Ala357=
ENST00000700417.1:c.1087_1097delinsGCCTCTGTGAT	ENSP00000514981.1:p.Ala363=
ENST00000700444.1:c.*928_*938delinsGCCTCTGTGAT	ENSP00000514992.1:n.*928_*938delinsGCCTCTGTGAT
ENST00000303635.12:c.1159_1169delinsGCCTCTGTGAT MANE Select	ENSP00000306522.6:p.Ala387=
ENST00000303635.11:c.1159_1169delinsGCCTCTGTGAT	ENSP00000306522.6:p.Ala387=
NM_015215.3:c.1159_1169delinsGCCTCTGTGAT	NP_056030.1:p.Ala387=
XM_011541083.1:c.1159_1169delinsGCCTCTGTGAT	XP_011539385.1:p.Ala387=
XM_011541084.1:c.1159_1169delinsGCCTCTGTGAT	XP_011539386.1:p.Ala387=
XM_011541085.1:c.1147_1157delinsGCCTCTGTGAT	XP_011539387.1:p.Ala383=
XM_011541086.1:c.1159_1169delinsGCCTCTGTGAT	XP_011539388.1:p.Ala387=
XM_011541087.1:c.1087_1097delinsGCCTCTGTGAT	XP_011539389.1:p.Ala363=
XM_011541088.1:c.1069_1079delinsGCCTCTGTGAT	XP_011539390.1:p.Ala357=
XM_011541089.1:c.1159_1169delinsGCCTCTGTGAT	XP_011539391.1:p.Ala387=
XM_011541090.1:c.1159_1169delinsGCCTCTGTGAT	XP_011539392.1:p.Ala387=
XM_011541091.1:c.1159_1169delinsGCCTCTGTGAT	XP_011539393.1:p.Ala387=
XM_011541092.1:c.1159_1169delinsGCCTCTGTGAT	XP_011539394.1:p.Ala387=
NM_001349608.1:c.1069_1079delinsGCCTCTGTGAT	NP_001336537.1:p.Ala357=
NM_001349609.1:c.1159_1169delinsGCCTCTGTGAT	NP_001336538.1:p.Ala387=
NM_001349610.1:c.1159_1169delinsGCCTCTGTGAT	NP_001336539.1:p.Ala387=
NM_001349612.1:c.1069_1079delinsGCCTCTGTGAT	NP_001336541.1:p.Ala357=
XM_011541083.2:c.1159_1169delinsGCCTCTGTGAT	XP_011539385.1:p.Ala387=
XM_011541084.2:c.1159_1169delinsGCCTCTGTGAT	XP_011539386.1:p.Ala387=
XM_011541086.3:c.1159_1169delinsGCCTCTGTGAT	XP_011539388.1:p.Ala387=
XM_011541087.2:c.1087_1097delinsGCCTCTGTGAT	XP_011539389.1:p.Ala363=
XM_011541088.2:c.1069_1079delinsGCCTCTGTGAT	XP_011539390.1:p.Ala357=
XM_011541090.3:c.1159_1169delinsGCCTCTGTGAT	XP_011539392.1:p.Ala387=
XM_011541091.2:c.1159_1169delinsGCCTCTGTGAT	XP_011539393.1:p.Ala387=
XM_011541092.3:c.1159_1169delinsGCCTCTGTGAT	XP_011539394.1:p.Ala387=
XM_017000774.2:c.1159_1169delinsGCCTCTGTGAT	XP_016856263.1:p.Ala387=
XM_017000777.1:c.1159_1169delinsGCCTCTGTGAT	XP_016856266.1:p.Ala387=
XM_017000778.1:c.1159_1169delinsGCCTCTGTGAT	XP_016856267.1:p.Ala387=
NM_015215.4:c.1159_1169delinsGCCTCTGTGAT MANE Select	NP_056030.1:p.Ala387=
NM_001349608.2:c.1069_1079delinsGCCTCTGTGAT	NP_001336537.1:p.Ala357=
NM_001349609.2:c.1159_1169delinsGCCTCTGTGAT	NP_001336538.1:p.Ala387=
NM_001349610.2:c.1159_1169delinsGCCTCTGTGAT	NP_001336539.1:p.Ala387=
NM_001349612.2:c.1069_1079delinsGCCTCTGTGAT	NP_001336541.1:p.Ala357=