Canonical Allele Identifier: CA2662133587

Gene: TTN

Linked Data

• gnomAD v4: 2-178621760-CAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178621763_178621765del , CM000664.2:g.178621763_178621765del	GRCh38
NC_000002.11:g.179486490_179486492del , CM000664.1:g.179486490_179486492del	GRCh37
NC_000002.10:g.179194735_179194737del	NCBI36
NG_011618.3:g.214040_214042del , LRG_391:g.214040_214042del
NG_051363.1:g.103937_103939del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.37379-22_37379-20del	ENSP00000343764.6:n.37379-22_37379-20del
ENST00000342175.11:c.18464-22_18464-20del	ENSP00000340554.6:n.18464-22_18464-20del
ENST00000359218.10:c.18263-22_18263-20del	ENSP00000352154.5:n.18263-22_18263-20del
ENST00000342175.10:c.18464-22_18464-20del	ENSP00000340554.6:n.18464-22_18464-20del
ENST00000342992.10:c.37379-22_37379-20del	ENSP00000343764.6:n.37379-22_37379-20del
ENST00000359218.9:c.18263-22_18263-20del	ENSP00000352154.5:n.18263-22_18263-20del
ENST00000460472.6:c.17888-22_17888-20del	ENSP00000434586.1:n.17888-22_17888-20del
ENST00000589042.5:c.45083-22_45083-20del MANE Select	ENSP00000467141.1:n.45083-22_45083-20del
ENST00000591111.5:c.40160-22_40160-20del	ENSP00000465570.1:n.40160-22_40160-20del
ENST00000615779.4:c.40160-22_40160-20del	ENSP00000483597.1:n.40160-22_40160-20del
NM_001256850.1:c.40160-22_40160-20del	NP_001243779.1:n.40160-22_40160-20del
NM_001267550.2:c.45083-22_45083-20del MANE Select	NP_001254479.2:n.45083-22_45083-20del
NM_003319.4:c.17888-22_17888-20del	NP_003310.4:n.17888-22_17888-20del
NM_133378.4:c.37379-22_37379-20del	NP_596869.4:n.37379-22_37379-20del
NM_133432.3:c.18263-22_18263-20del	NP_597676.3:n.18263-22_18263-20del
NM_133437.4:c.18464-22_18464-20del	NP_597681.4:n.18464-22_18464-20del
XM_011511729.1:c.44180-22_44180-20del	XP_011510031.1:n.44180-22_44180-20del
XM_011511730.1:c.18074-22_18074-20del	XP_011510032.1:n.18074-22_18074-20del
XM_011511731.1:c.17933-22_17933-20del	XP_011510033.1:n.17933-22_17933-20del
XM_017004819.1:c.43976-22_43976-20del	XP_016860308.1:n.43976-22_43976-20del
XM_017004820.1:c.39374-22_39374-20del	XP_016860309.1:n.39374-22_39374-20del
XM_017004821.1:c.39371-22_39371-20del	XP_016860310.1:n.39371-22_39371-20del
XM_017004822.1:c.36413-22_36413-20del	XP_016860311.1:n.36413-22_36413-20del
XM_017004823.1:c.18029-22_18029-20del	XP_016860312.1:n.18029-22_18029-20del
XM_024453094.1:c.39524-22_39524-20del	XP_024308862.1:n.39524-22_39524-20del
XM_024453095.1:c.39521-22_39521-20del	XP_024308863.1:n.39521-22_39521-20del
XM_024453096.1:c.38954-22_38954-20del	XP_024308864.1:n.38954-22_38954-20del
XM_024453097.1:c.36296-22_36296-20del	XP_024308865.1:n.36296-22_36296-20del
XM_024453098.1:c.36215-22_36215-20del	XP_024308866.1:n.36215-22_36215-20del
XM_024453099.1:c.17978-22_17978-20del	XP_024308867.1:n.17978-22_17978-20del
XM_024453100.1:c.7832-22_7832-20del	XP_024308868.1:n.7832-22_7832-20del