Canonical Allele Identifier: CA349601350

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179432122T>C (hg19) ; chr2:g.178567395T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178567395T>C , CM000664.2:g.178567395T>C	GRCh38
NC_000002.11:g.179432122T>C , CM000664.1:g.179432122T>C	GRCh37
NC_000002.10:g.179140368T>C	NCBI36
NG_011618.3:g.268408A>G , LRG_391:g.268408A>G
NG_051363.1:g.49569T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.71033A>G (TTN)	ENSP00000343764.6:p.Asp23678Gly
ENST00000342175.11:c.52118A>G (TTN)	ENSP00000340554.6:p.Asp17373Gly
ENST00000359218.10:c.51917A>G (TTN)	ENSP00000352154.5:p.Asp17306Gly
ENST00000342175.10:c.52118A>G (TTN)	ENSP00000340554.6:p.Asp17373Gly
ENST00000342992.10:c.71033A>G (TTN)	ENSP00000343764.6:p.Asp23678Gly
ENST00000359218.9:c.51917A>G (TTN)	ENSP00000352154.5:p.Asp17306Gly
ENST00000460472.6:c.51542A>G (TTN)	ENSP00000434586.1:p.Asp17181Gly
ENST00000589042.5:c.78737A>G (TTN) MANE Select	ENSP00000467141.1:p.Asp26246Gly
ENST00000591111.5:c.73814A>G (TTN)	ENSP00000465570.1:p.Asp24605Gly
ENST00000615779.4:c.73814A>G (TTN)	ENSP00000483597.1:p.Asp24605Gly
NM_001256850.1:c.73814A>G (TTN)	NP_001243779.1:p.Asp24605Gly
NM_001267550.2:c.78737A>G (TTN) MANE Select	NP_001254479.2:p.Asp26246Gly
NM_003319.4:c.51542A>G (TTN)	NP_003310.4:p.Asp17181Gly
NM_133378.4:c.71033A>G (TTN)	NP_596869.4:p.Asp23678Gly
NM_133432.3:c.51917A>G (TTN)	NP_597676.3:p.Asp17306Gly
NM_133437.4:c.52118A>G (TTN)	NP_597681.4:p.Asp17373Gly
NR_038271.1:n.447-3905T>C (TTN-AS1)
NR_038272.1:n.2044-15177T>C (TTN-AS1)
XM_011511729.1:c.77834A>G (TTN)	XP_011510031.1:p.Asp25945Gly
XM_011511730.1:c.51728A>G (TTN)	XP_011510032.1:p.Asp17243Gly
XM_011511731.1:c.51587A>G (TTN)	XP_011510033.1:p.Asp17196Gly
XM_017004819.1:c.77630A>G (TTN)	XP_016860308.1:p.Asp25877Gly
XM_017004820.1:c.73028A>G (TTN)	XP_016860309.1:p.Asp24343Gly
XM_017004821.1:c.73025A>G (TTN)	XP_016860310.1:p.Asp24342Gly
XM_017004822.1:c.70067A>G (TTN)	XP_016860311.1:p.Asp23356Gly
XM_017004823.1:c.51683A>G (TTN)	XP_016860312.1:p.Asp17228Gly
XM_024453094.1:c.73178A>G (TTN)	XP_024308862.1:p.Asp24393Gly
XM_024453095.1:c.73175A>G (TTN)	XP_024308863.1:p.Asp24392Gly
XM_024453096.1:c.72608A>G (TTN)	XP_024308864.1:p.Asp24203Gly
XM_024453097.1:c.69950A>G (TTN)	XP_024308865.1:p.Asp23317Gly
XM_024453098.1:c.69869A>G (TTN)	XP_024308866.1:p.Asp23290Gly
XM_024453099.1:c.51632A>G (TTN)	XP_024308867.1:p.Asp17211Gly
XM_024453100.1:c.41486A>G (TTN)	XP_024308868.1:p.Asp13829Gly