Canonical Allele Identifier: CA349406656

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395144T>A (hg19) ; chr2:g.178530417T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530417T>A , CM000664.2:g.178530417T>A	GRCh38
NC_000002.11:g.179395144T>A , CM000664.1:g.179395144T>A	GRCh37
NC_000002.10:g.179103390T>A	NCBI36
NG_011618.3:g.305386A>T , LRG_391:g.305386A>T
NG_051363.1:g.12591T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98494A>T (TTN)	ENSP00000343764.6:p.Thr32832Ser
ENST00000342175.11:c.79579A>T (TTN)	ENSP00000340554.6:p.Thr26527Ser
ENST00000359218.10:c.79378A>T (TTN)	ENSP00000352154.5:p.Thr26460Ser
ENST00000342175.10:c.79579A>T (TTN)	ENSP00000340554.6:p.Thr26527Ser
ENST00000342992.10:c.98494A>T (TTN)	ENSP00000343764.6:p.Thr32832Ser
ENST00000359218.9:c.79378A>T (TTN)	ENSP00000352154.5:p.Thr26460Ser
ENST00000460472.6:c.79003A>T (TTN)	ENSP00000434586.1:p.Thr26335Ser
ENST00000589042.5:c.106198A>T (TTN) MANE Select	ENSP00000467141.1:p.Thr35400Ser
ENST00000591111.5:c.101275A>T (TTN)	ENSP00000465570.1:p.Thr33759Ser
ENST00000615779.4:c.101275A>T (TTN)	ENSP00000483597.1:p.Thr33759Ser
NM_001256850.1:c.101275A>T (TTN)	NP_001243779.1:p.Thr33759Ser
NM_001267550.2:c.106198A>T (TTN) MANE Select	NP_001254479.2:p.Thr35400Ser
NM_003319.4:c.79003A>T (TTN)	NP_003310.4:p.Thr26335Ser
NM_133378.4:c.98494A>T (TTN)	NP_596869.4:p.Thr32832Ser
NM_133432.3:c.79378A>T (TTN)	NP_597676.3:p.Thr26460Ser
NM_133437.4:c.79579A>T (TTN)	NP_597681.4:p.Thr26527Ser
NR_038271.1:n.446+6781T>A (TTN-AS1)
NR_038272.1:n.220-5315T>A (TTN-AS1)
XM_011511729.1:c.105295A>T (TTN)	XP_011510031.1:p.Thr35099Ser
XM_011511730.1:c.79189A>T (TTN)	XP_011510032.1:p.Thr26397Ser
XM_011511731.1:c.79048A>T (TTN)	XP_011510033.1:p.Thr26350Ser
XM_017004819.1:c.105091A>T (TTN)	XP_016860308.1:p.Thr35031Ser
XM_017004820.1:c.100489A>T (TTN)	XP_016860309.1:p.Thr33497Ser
XM_017004821.1:c.100486A>T (TTN)	XP_016860310.1:p.Thr33496Ser
XM_017004822.1:c.97528A>T (TTN)	XP_016860311.1:p.Thr32510Ser
XM_017004823.1:c.79144A>T (TTN)	XP_016860312.1:p.Thr26382Ser
XM_024453094.1:c.100639A>T (TTN)	XP_024308862.1:p.Thr33547Ser
XM_024453095.1:c.100636A>T (TTN)	XP_024308863.1:p.Thr33546Ser
XM_024453096.1:c.100069A>T (TTN)	XP_024308864.1:p.Thr33357Ser
XM_024453097.1:c.97411A>T (TTN)	XP_024308865.1:p.Thr32471Ser
XM_024453098.1:c.97330A>T (TTN)	XP_024308866.1:p.Thr32444Ser
XM_024453099.1:c.79093A>T (TTN)	XP_024308867.1:p.Thr26365Ser
XM_024453100.1:c.68947A>T (TTN)	XP_024308868.1:p.Thr22983Ser