Canonical Allele Identifier: CA1310552337

Gene: TTN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178621753_178621754delinsGA , CM000664.2:g.178621753_178621754delinsGA	GRCh38
NC_000002.11:g.179486480_179486481delinsGA , CM000664.1:g.179486480_179486481delinsGA	GRCh37
NC_000002.10:g.179194725_179194726delinsGA	NCBI36
NG_011618.3:g.214049_214050delinsTC , LRG_391:g.214049_214050delinsTC
NG_051363.1:g.103927_103928delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.37379-13_37379-12delinsTC	ENSP00000343764.6:n.37379-13_37379-12delinsTC
ENST00000342175.11:c.18464-13_18464-12delinsTC	ENSP00000340554.6:n.18464-13_18464-12delinsTC
ENST00000359218.10:c.18263-13_18263-12delinsTC	ENSP00000352154.5:n.18263-13_18263-12delinsTC
ENST00000342175.10:c.18464-13_18464-12delinsTC	ENSP00000340554.6:n.18464-13_18464-12delinsTC
ENST00000342992.10:c.37379-13_37379-12delinsTC	ENSP00000343764.6:n.37379-13_37379-12delinsTC
ENST00000359218.9:c.18263-13_18263-12delinsTC	ENSP00000352154.5:n.18263-13_18263-12delinsTC
ENST00000460472.6:c.17888-13_17888-12delinsTC	ENSP00000434586.1:n.17888-13_17888-12delinsTC
ENST00000589042.5:c.45083-13_45083-12delinsTC MANE Select	ENSP00000467141.1:n.45083-13_45083-12delinsTC
ENST00000591111.5:c.40160-13_40160-12delinsTC	ENSP00000465570.1:n.40160-13_40160-12delinsTC
ENST00000615779.4:c.40160-13_40160-12delinsTC	ENSP00000483597.1:n.40160-13_40160-12delinsTC
NM_001256850.1:c.40160-13_40160-12delinsTC	NP_001243779.1:n.40160-13_40160-12delinsTC
NM_001267550.2:c.45083-13_45083-12delinsTC MANE Select	NP_001254479.2:n.45083-13_45083-12delinsTC
NM_003319.4:c.17888-13_17888-12delinsTC	NP_003310.4:n.17888-13_17888-12delinsTC
NM_133378.4:c.37379-13_37379-12delinsTC	NP_596869.4:n.37379-13_37379-12delinsTC
NM_133432.3:c.18263-13_18263-12delinsTC	NP_597676.3:n.18263-13_18263-12delinsTC
NM_133437.4:c.18464-13_18464-12delinsTC	NP_597681.4:n.18464-13_18464-12delinsTC
XM_011511729.1:c.44180-13_44180-12delinsTC	XP_011510031.1:n.44180-13_44180-12delinsTC
XM_011511730.1:c.18074-13_18074-12delinsTC	XP_011510032.1:n.18074-13_18074-12delinsTC
XM_011511731.1:c.17933-13_17933-12delinsTC	XP_011510033.1:n.17933-13_17933-12delinsTC
XM_017004819.1:c.43976-13_43976-12delinsTC	XP_016860308.1:n.43976-13_43976-12delinsTC
XM_017004820.1:c.39374-13_39374-12delinsTC	XP_016860309.1:n.39374-13_39374-12delinsTC
XM_017004821.1:c.39371-13_39371-12delinsTC	XP_016860310.1:n.39371-13_39371-12delinsTC
XM_017004822.1:c.36413-13_36413-12delinsTC	XP_016860311.1:n.36413-13_36413-12delinsTC
XM_017004823.1:c.18029-13_18029-12delinsTC	XP_016860312.1:n.18029-13_18029-12delinsTC
XM_024453094.1:c.39524-13_39524-12delinsTC	XP_024308862.1:n.39524-13_39524-12delinsTC
XM_024453095.1:c.39521-13_39521-12delinsTC	XP_024308863.1:n.39521-13_39521-12delinsTC
XM_024453096.1:c.38954-13_38954-12delinsTC	XP_024308864.1:n.38954-13_38954-12delinsTC
XM_024453097.1:c.36296-13_36296-12delinsTC	XP_024308865.1:n.36296-13_36296-12delinsTC
XM_024453098.1:c.36215-13_36215-12delinsTC	XP_024308866.1:n.36215-13_36215-12delinsTC
XM_024453099.1:c.17978-13_17978-12delinsTC	XP_024308867.1:n.17978-13_17978-12delinsTC
XM_024453100.1:c.7832-13_7832-12delinsTC	XP_024308868.1:n.7832-13_7832-12delinsTC