Canonical Allele Identifier: CA2740107133

Gene: CAMTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.7468679_7468680insGTTT , CM000663.2:g.7468679_7468680insGTTT	GRCh38
NC_000001.10:g.7528739_7528740insGTTT , CM000663.1:g.7528739_7528740insGTTT	GRCh37
NC_000001.9:g.7451326_7451327insGTTT	NCBI36
NG_053148.1:g.688356_688357insGTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476864.2:c.510+778_510+779insGTTT	ENSP00000452319.2:n.510+778_510+779insGTTT
ENST00000700414.1:c.*361+778_*361+779insGTTT	ENSP00000514978.1:n.*361+778_*361+779insGTTT
ENST00000700415.1:c.420+778_420+779insGTTT	ENSP00000514979.1:n.420+778_420+779insGTTT
ENST00000700417.1:c.439-171721_439-171720insGTTT	ENSP00000514981.1:n.439-171721_439-171720insGTTT
ENST00000700444.1:c.*280-171721_*280-171720insGTTT	ENSP00000514992.1:n.*280-171721_*280-171720insGTTT
ENST00000303635.12:c.510+778_510+779insGTTT MANE Select	ENSP00000306522.6:n.510+778_510+779insGTTT
ENST00000303635.11:c.510+778_510+779insGTTT	ENSP00000306522.6:n.510+778_510+779insGTTT
NM_015215.3:c.510+778_510+779insGTTT	NP_056030.1:n.510+778_510+779insGTTT
XM_011541083.1:c.510+778_510+779insGTTT	XP_011539385.1:n.510+778_510+779insGTTT
XM_011541084.1:c.510+778_510+779insGTTT	XP_011539386.1:n.510+778_510+779insGTTT
XM_011541085.1:c.498+778_498+779insGTTT	XP_011539387.1:n.498+778_498+779insGTTT
XM_011541086.1:c.510+778_510+779insGTTT	XP_011539388.1:n.510+778_510+779insGTTT
XM_011541087.1:c.439-171721_439-171720insGTTT	XP_011539389.1:n.439-171721_439-171720insGTTT
XM_011541088.1:c.420+778_420+779insGTTT	XP_011539390.1:n.420+778_420+779insGTTT
XM_011541089.1:c.510+778_510+779insGTTT	XP_011539391.1:n.510+778_510+779insGTTT
XM_011541090.1:c.510+778_510+779insGTTT	XP_011539392.1:n.510+778_510+779insGTTT
XM_011541091.1:c.510+778_510+779insGTTT	XP_011539393.1:n.510+778_510+779insGTTT
XM_011541092.1:c.510+778_510+779insGTTT	XP_011539394.1:n.510+778_510+779insGTTT
NM_001349608.1:c.420+778_420+779insGTTT	NP_001336537.1:n.420+778_420+779insGTTT
NM_001349609.1:c.510+778_510+779insGTTT	NP_001336538.1:n.510+778_510+779insGTTT
NM_001349610.1:c.510+778_510+779insGTTT	NP_001336539.1:n.510+778_510+779insGTTT
NM_001349612.1:c.420+778_420+779insGTTT	NP_001336541.1:n.420+778_420+779insGTTT
XM_011541083.2:c.510+778_510+779insGTTT	XP_011539385.1:n.510+778_510+779insGTTT
XM_011541084.2:c.510+778_510+779insGTTT	XP_011539386.1:n.510+778_510+779insGTTT
XM_011541086.3:c.510+778_510+779insGTTT	XP_011539388.1:n.510+778_510+779insGTTT
XM_011541087.2:c.439-171721_439-171720insGTTT	XP_011539389.1:n.439-171721_439-171720insGTTT
XM_011541088.2:c.420+778_420+779insGTTT	XP_011539390.1:n.420+778_420+779insGTTT
XM_011541090.3:c.510+778_510+779insGTTT	XP_011539392.1:n.510+778_510+779insGTTT
XM_011541091.2:c.510+778_510+779insGTTT	XP_011539393.1:n.510+778_510+779insGTTT
XM_011541092.3:c.510+778_510+779insGTTT	XP_011539394.1:n.510+778_510+779insGTTT
XM_017000774.2:c.510+778_510+779insGTTT	XP_016856263.1:n.510+778_510+779insGTTT
XM_017000777.1:c.510+778_510+779insGTTT	XP_016856266.1:n.510+778_510+779insGTTT
XM_017000778.1:c.510+778_510+779insGTTT	XP_016856267.1:n.510+778_510+779insGTTT
NM_015215.4:c.510+778_510+779insGTTT MANE Select	NP_056030.1:n.510+778_510+779insGTTT
NM_001349608.2:c.420+778_420+779insGTTT	NP_001336537.1:n.420+778_420+779insGTTT
NM_001349609.2:c.510+778_510+779insGTTT	NP_001336538.1:n.510+778_510+779insGTTT
NM_001349610.2:c.510+778_510+779insGTTT	NP_001336539.1:n.510+778_510+779insGTTT
NM_001349612.2:c.420+778_420+779insGTTT	NP_001336541.1:n.420+778_420+779insGTTT