Canonical Allele Identifier: CA2662130844

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178591943-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591943A>G , CM000664.2:g.178591943A>G	GRCh38
NC_000002.11:g.179456670A>G , CM000664.1:g.179456670A>G	GRCh37
NC_000002.10:g.179164916A>G	NCBI36
NG_011618.3:g.243860T>C , LRG_391:g.243860T>C
NG_051363.1:g.74117A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.52222+35T>C (TTN)	ENSP00000343764.6:n.52222+35T>C
ENST00000342175.11:c.33307+35T>C (TTN)	ENSP00000340554.6:n.33307+35T>C
ENST00000359218.10:c.33106+35T>C (TTN)	ENSP00000352154.5:n.33106+35T>C
ENST00000342175.10:c.33307+35T>C (TTN)	ENSP00000340554.6:n.33307+35T>C
ENST00000342992.10:c.52222+35T>C (TTN)	ENSP00000343764.6:n.52222+35T>C
ENST00000359218.9:c.33106+35T>C (TTN)	ENSP00000352154.5:n.33106+35T>C
ENST00000460472.6:c.32731+35T>C (TTN)	ENSP00000434586.1:n.32731+35T>C
ENST00000589042.5:c.59926+35T>C (TTN) MANE Select	ENSP00000467141.1:n.59926+35T>C
ENST00000591111.5:c.55003+35T>C (TTN)	ENSP00000465570.1:n.55003+35T>C
ENST00000615779.4:c.55003+35T>C (TTN)	ENSP00000483597.1:n.55003+35T>C
NM_001256850.1:c.55003+35T>C (TTN)	NP_001243779.1:n.55003+35T>C
NM_001267550.2:c.59926+35T>C (TTN) MANE Select	NP_001254479.2:n.59926+35T>C
NM_003319.4:c.32731+35T>C (TTN)	NP_003310.4:n.32731+35T>C
NM_133378.4:c.52222+35T>C (TTN)	NP_596869.4:n.52222+35T>C
NM_133432.3:c.33106+35T>C (TTN)	NP_597676.3:n.33106+35T>C
NM_133437.4:c.33307+35T>C (TTN)	NP_597681.4:n.33307+35T>C
NR_038271.1:n.597-5653A>G (TTN-AS1)
NR_038272.1:n.3364+629A>G (TTN-AS1)
XM_011511729.1:c.59023+35T>C (TTN)	XP_011510031.1:n.59023+35T>C
XM_011511730.1:c.32917+35T>C (TTN)	XP_011510032.1:n.32917+35T>C
XM_011511731.1:c.32776+35T>C (TTN)	XP_011510033.1:n.32776+35T>C
XM_017004819.1:c.58819+35T>C (TTN)	XP_016860308.1:n.58819+35T>C
XM_017004820.1:c.54217+35T>C (TTN)	XP_016860309.1:n.54217+35T>C
XM_017004821.1:c.54214+35T>C (TTN)	XP_016860310.1:n.54214+35T>C
XM_017004822.1:c.51256+35T>C (TTN)	XP_016860311.1:n.51256+35T>C
XM_017004823.1:c.32872+35T>C (TTN)	XP_016860312.1:n.32872+35T>C
XM_024453094.1:c.54367+35T>C (TTN)	XP_024308862.1:n.54367+35T>C
XM_024453095.1:c.54364+35T>C (TTN)	XP_024308863.1:n.54364+35T>C
XM_024453096.1:c.53797+35T>C (TTN)	XP_024308864.1:n.53797+35T>C
XM_024453097.1:c.51139+35T>C (TTN)	XP_024308865.1:n.51139+35T>C
XM_024453098.1:c.51058+35T>C (TTN)	XP_024308866.1:n.51058+35T>C
XM_024453099.1:c.32821+35T>C (TTN)	XP_024308867.1:n.32821+35T>C
XM_024453100.1:c.22675+35T>C (TTN)	XP_024308868.1:n.22675+35T>C