Canonical Allele Identifier: CA538435872

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1363502764
• gnomAD v2: 2-179482822-CAGA-C
• gnomAD v4: 2-178618095-CAGA-C
• MyVariant Identifiers: chr2:g.179482823_179482825del (hg19) ; chr2:g.178618096_178618098del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618103_178618105del , CM000664.2:g.178618103_178618105del	GRCh38
NC_000002.11:g.179482830_179482832del , CM000664.1:g.179482830_179482832del	GRCh37
NC_000002.10:g.179191075_179191077del	NCBI36
NG_011618.3:g.217705_217707del , LRG_391:g.217705_217707del
NG_051363.1:g.100277_100279del

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.39566-17_39566-15del (TTN)	ENSP00000343764.6:n.39566-17_39566-15del
ENST00000342175.11:c.20651-17_20651-15del (TTN)	ENSP00000340554.6:n.20651-17_20651-15del
ENST00000359218.10:c.20450-17_20450-15del (TTN)	ENSP00000352154.5:n.20450-17_20450-15del
ENST00000342175.10:c.20651-17_20651-15del (TTN)	ENSP00000340554.6:n.20651-17_20651-15del
ENST00000342992.10:c.39566-17_39566-15del (TTN)	ENSP00000343764.6:n.39566-17_39566-15del
ENST00000359218.9:c.20450-17_20450-15del (TTN)	ENSP00000352154.5:n.20450-17_20450-15del
ENST00000460472.6:c.20075-17_20075-15del (TTN)	ENSP00000434586.1:n.20075-17_20075-15del
ENST00000589042.5:c.47270-17_47270-15del (TTN) MANE Select	ENSP00000467141.1:n.47270-17_47270-15del
ENST00000591111.5:c.42347-17_42347-15del (TTN)	ENSP00000465570.1:n.42347-17_42347-15del
ENST00000615779.4:c.42347-17_42347-15del (TTN)	ENSP00000483597.1:n.42347-17_42347-15del
NM_001256850.1:c.42347-17_42347-15del (TTN)	NP_001243779.1:n.42347-17_42347-15del
NM_001267550.2:c.47270-17_47270-15del (TTN) MANE Select	NP_001254479.2:n.47270-17_47270-15del
NM_003319.4:c.20075-17_20075-15del (TTN)	NP_003310.4:n.20075-17_20075-15del
NM_133378.4:c.39566-17_39566-15del (TTN)	NP_596869.4:n.39566-17_39566-15del
NM_133432.3:c.20450-17_20450-15del (TTN)	NP_597676.3:n.20450-17_20450-15del
NM_133437.4:c.20651-17_20651-15del (TTN)	NP_597681.4:n.20651-17_20651-15del
NR_038271.1:n.1605-1650_1605-1648del (TTN-AS1)
XM_011511729.1:c.46367-17_46367-15del (TTN)	XP_011510031.1:n.46367-17_46367-15del
XM_011511730.1:c.20261-17_20261-15del (TTN)	XP_011510032.1:n.20261-17_20261-15del
XM_011511731.1:c.20120-17_20120-15del (TTN)	XP_011510033.1:n.20120-17_20120-15del
XM_017004819.1:c.46163-17_46163-15del (TTN)	XP_016860308.1:n.46163-17_46163-15del
XM_017004820.1:c.41561-17_41561-15del (TTN)	XP_016860309.1:n.41561-17_41561-15del
XM_017004821.1:c.41558-17_41558-15del (TTN)	XP_016860310.1:n.41558-17_41558-15del
XM_017004822.1:c.38600-17_38600-15del (TTN)	XP_016860311.1:n.38600-17_38600-15del
XM_017004823.1:c.20216-17_20216-15del (TTN)	XP_016860312.1:n.20216-17_20216-15del
XM_024453094.1:c.41711-17_41711-15del (TTN)	XP_024308862.1:n.41711-17_41711-15del
XM_024453095.1:c.41708-17_41708-15del (TTN)	XP_024308863.1:n.41708-17_41708-15del
XM_024453096.1:c.41141-17_41141-15del (TTN)	XP_024308864.1:n.41141-17_41141-15del
XM_024453097.1:c.38483-17_38483-15del (TTN)	XP_024308865.1:n.38483-17_38483-15del
XM_024453098.1:c.38402-17_38402-15del (TTN)	XP_024308866.1:n.38402-17_38402-15del
XM_024453099.1:c.20165-17_20165-15del (TTN)	XP_024308867.1:n.20165-17_20165-15del
XM_024453100.1:c.10019-17_10019-15del (TTN)	XP_024308868.1:n.10019-17_10019-15del