Canonical Allele Identifier: CA349405332

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394791A>T (hg19) ; chr2:g.178530064A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530064A>T , CM000664.2:g.178530064A>T	GRCh38
NC_000002.11:g.179394791A>T , CM000664.1:g.179394791A>T	GRCh37
NC_000002.10:g.179103037A>T	NCBI36
NG_011618.3:g.305739T>A , LRG_391:g.305739T>A
NG_051363.1:g.12238A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98723T>A (TTN)	ENSP00000343764.6:p.Phe32908Tyr
ENST00000342175.11:c.79808T>A (TTN)	ENSP00000340554.6:p.Phe26603Tyr
ENST00000359218.10:c.79607T>A (TTN)	ENSP00000352154.5:p.Phe26536Tyr
ENST00000342175.10:c.79808T>A (TTN)	ENSP00000340554.6:p.Phe26603Tyr
ENST00000342992.10:c.98723T>A (TTN)	ENSP00000343764.6:p.Phe32908Tyr
ENST00000359218.9:c.79607T>A (TTN)	ENSP00000352154.5:p.Phe26536Tyr
ENST00000460472.6:c.79232T>A (TTN)	ENSP00000434586.1:p.Phe26411Tyr
ENST00000589042.5:c.106427T>A (TTN) MANE Select	ENSP00000467141.1:p.Phe35476Tyr
ENST00000591111.5:c.101504T>A (TTN)	ENSP00000465570.1:p.Phe33835Tyr
ENST00000615779.4:c.101504T>A (TTN)	ENSP00000483597.1:p.Phe33835Tyr
NM_001256850.1:c.101504T>A (TTN)	NP_001243779.1:p.Phe33835Tyr
NM_001267550.2:c.106427T>A (TTN) MANE Select	NP_001254479.2:p.Phe35476Tyr
NM_003319.4:c.79232T>A (TTN)	NP_003310.4:p.Phe26411Tyr
NM_133378.4:c.98723T>A (TTN)	NP_596869.4:p.Phe32908Tyr
NM_133432.3:c.79607T>A (TTN)	NP_597676.3:p.Phe26536Tyr
NM_133437.4:c.79808T>A (TTN)	NP_597681.4:p.Phe26603Tyr
NR_038271.1:n.446+6428A>T (TTN-AS1)
NR_038272.1:n.220-5668A>T (TTN-AS1)
XM_011511729.1:c.105524T>A (TTN)	XP_011510031.1:p.Phe35175Tyr
XM_011511730.1:c.79418T>A (TTN)	XP_011510032.1:p.Phe26473Tyr
XM_011511731.1:c.79277T>A (TTN)	XP_011510033.1:p.Phe26426Tyr
XM_017004819.1:c.105320T>A (TTN)	XP_016860308.1:p.Phe35107Tyr
XM_017004820.1:c.100718T>A (TTN)	XP_016860309.1:p.Phe33573Tyr
XM_017004821.1:c.100715T>A (TTN)	XP_016860310.1:p.Phe33572Tyr
XM_017004822.1:c.97757T>A (TTN)	XP_016860311.1:p.Phe32586Tyr
XM_017004823.1:c.79373T>A (TTN)	XP_016860312.1:p.Phe26458Tyr
XM_024453094.1:c.100868T>A (TTN)	XP_024308862.1:p.Phe33623Tyr
XM_024453095.1:c.100865T>A (TTN)	XP_024308863.1:p.Phe33622Tyr
XM_024453096.1:c.100298T>A (TTN)	XP_024308864.1:p.Phe33433Tyr
XM_024453097.1:c.97640T>A (TTN)	XP_024308865.1:p.Phe32547Tyr
XM_024453098.1:c.97559T>A (TTN)	XP_024308866.1:p.Phe32520Tyr
XM_024453099.1:c.79322T>A (TTN)	XP_024308867.1:p.Phe26441Tyr
XM_024453100.1:c.69176T>A (TTN)	XP_024308868.1:p.Phe23059Tyr