Canonical Allele Identifier: CA349405614

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394836G>T (hg19) ; chr2:g.178530109G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530109G>T , CM000664.2:g.178530109G>T	GRCh38
NC_000002.11:g.179394836G>T , CM000664.1:g.179394836G>T	GRCh37
NC_000002.10:g.179103082G>T	NCBI36
NG_011618.3:g.305694C>A , LRG_391:g.305694C>A
NG_051363.1:g.12283G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98678C>A (TTN)	ENSP00000343764.6:p.Thr32893Lys
ENST00000342175.11:c.79763C>A (TTN)	ENSP00000340554.6:p.Thr26588Lys
ENST00000359218.10:c.79562C>A (TTN)	ENSP00000352154.5:p.Thr26521Lys
ENST00000342175.10:c.79763C>A (TTN)	ENSP00000340554.6:p.Thr26588Lys
ENST00000342992.10:c.98678C>A (TTN)	ENSP00000343764.6:p.Thr32893Lys
ENST00000359218.9:c.79562C>A (TTN)	ENSP00000352154.5:p.Thr26521Lys
ENST00000460472.6:c.79187C>A (TTN)	ENSP00000434586.1:p.Thr26396Lys
ENST00000589042.5:c.106382C>A (TTN) MANE Select	ENSP00000467141.1:p.Thr35461Lys
ENST00000591111.5:c.101459C>A (TTN)	ENSP00000465570.1:p.Thr33820Lys
ENST00000615779.4:c.101459C>A (TTN)	ENSP00000483597.1:p.Thr33820Lys
NM_001256850.1:c.101459C>A (TTN)	NP_001243779.1:p.Thr33820Lys
NM_001267550.2:c.106382C>A (TTN) MANE Select	NP_001254479.2:p.Thr35461Lys
NM_003319.4:c.79187C>A (TTN)	NP_003310.4:p.Thr26396Lys
NM_133378.4:c.98678C>A (TTN)	NP_596869.4:p.Thr32893Lys
NM_133432.3:c.79562C>A (TTN)	NP_597676.3:p.Thr26521Lys
NM_133437.4:c.79763C>A (TTN)	NP_597681.4:p.Thr26588Lys
NR_038271.1:n.446+6473G>T (TTN-AS1)
NR_038272.1:n.220-5623G>T (TTN-AS1)
XM_011511729.1:c.105479C>A (TTN)	XP_011510031.1:p.Thr35160Lys
XM_011511730.1:c.79373C>A (TTN)	XP_011510032.1:p.Thr26458Lys
XM_011511731.1:c.79232C>A (TTN)	XP_011510033.1:p.Thr26411Lys
XM_017004819.1:c.105275C>A (TTN)	XP_016860308.1:p.Thr35092Lys
XM_017004820.1:c.100673C>A (TTN)	XP_016860309.1:p.Thr33558Lys
XM_017004821.1:c.100670C>A (TTN)	XP_016860310.1:p.Thr33557Lys
XM_017004822.1:c.97712C>A (TTN)	XP_016860311.1:p.Thr32571Lys
XM_017004823.1:c.79328C>A (TTN)	XP_016860312.1:p.Thr26443Lys
XM_024453094.1:c.100823C>A (TTN)	XP_024308862.1:p.Thr33608Lys
XM_024453095.1:c.100820C>A (TTN)	XP_024308863.1:p.Thr33607Lys
XM_024453096.1:c.100253C>A (TTN)	XP_024308864.1:p.Thr33418Lys
XM_024453097.1:c.97595C>A (TTN)	XP_024308865.1:p.Thr32532Lys
XM_024453098.1:c.97514C>A (TTN)	XP_024308866.1:p.Thr32505Lys
XM_024453099.1:c.79277C>A (TTN)	XP_024308867.1:p.Thr26426Lys
XM_024453100.1:c.69131C>A (TTN)	XP_024308868.1:p.Thr23044Lys