Canonical Allele Identifier: CA349446308

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408062T>A (hg19) ; chr2:g.178543335T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543335T>A , CM000664.2:g.178543335T>A	GRCh38
NC_000002.11:g.179408062T>A , CM000664.1:g.179408062T>A	GRCh37
NC_000002.10:g.179116308T>A	NCBI36
NG_011618.3:g.292468A>T , LRG_391:g.292468A>T
NG_051363.1:g.25509T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88934A>T (TTN)	ENSP00000343764.6:p.Asp29645Val
ENST00000342175.11:c.70019A>T (TTN)	ENSP00000340554.6:p.Asp23340Val
ENST00000359218.10:c.69818A>T (TTN)	ENSP00000352154.5:p.Asp23273Val
ENST00000342175.10:c.70019A>T (TTN)	ENSP00000340554.6:p.Asp23340Val
ENST00000342992.10:c.88934A>T (TTN)	ENSP00000343764.6:p.Asp29645Val
ENST00000359218.9:c.69818A>T (TTN)	ENSP00000352154.5:p.Asp23273Val
ENST00000460472.6:c.69443A>T (TTN)	ENSP00000434586.1:p.Asp23148Val
ENST00000589042.5:c.96638A>T (TTN) MANE Select	ENSP00000467141.1:p.Asp32213Val
ENST00000591111.5:c.91715A>T (TTN)	ENSP00000465570.1:p.Asp30572Val
ENST00000615779.4:c.91715A>T (TTN)	ENSP00000483597.1:p.Asp30572Val
NM_001256850.1:c.91715A>T (TTN)	NP_001243779.1:p.Asp30572Val
NM_001267550.2:c.96638A>T (TTN) MANE Select	NP_001254479.2:p.Asp32213Val
NM_003319.4:c.69443A>T (TTN)	NP_003310.4:p.Asp23148Val
NM_133378.4:c.88934A>T (TTN)	NP_596869.4:p.Asp29645Val
NM_133432.3:c.69818A>T (TTN)	NP_597676.3:p.Asp23273Val
NM_133437.4:c.70019A>T (TTN)	NP_597681.4:p.Asp23340Val
NR_038271.1:n.446+19699T>A (TTN-AS1)
NR_038272.1:n.2043+974T>A (TTN-AS1)
XM_011511729.1:c.95735A>T (TTN)	XP_011510031.1:p.Asp31912Val
XM_011511730.1:c.69629A>T (TTN)	XP_011510032.1:p.Asp23210Val
XM_011511731.1:c.69488A>T (TTN)	XP_011510033.1:p.Asp23163Val
XM_017004819.1:c.95531A>T (TTN)	XP_016860308.1:p.Asp31844Val
XM_017004820.1:c.90929A>T (TTN)	XP_016860309.1:p.Asp30310Val
XM_017004821.1:c.90926A>T (TTN)	XP_016860310.1:p.Asp30309Val
XM_017004822.1:c.87968A>T (TTN)	XP_016860311.1:p.Asp29323Val
XM_017004823.1:c.69584A>T (TTN)	XP_016860312.1:p.Asp23195Val
XM_024453094.1:c.91079A>T (TTN)	XP_024308862.1:p.Asp30360Val
XM_024453095.1:c.91076A>T (TTN)	XP_024308863.1:p.Asp30359Val
XM_024453096.1:c.90509A>T (TTN)	XP_024308864.1:p.Asp30170Val
XM_024453097.1:c.87851A>T (TTN)	XP_024308865.1:p.Asp29284Val
XM_024453098.1:c.87770A>T (TTN)	XP_024308866.1:p.Asp29257Val
XM_024453099.1:c.69533A>T (TTN)	XP_024308867.1:p.Asp23178Val
XM_024453100.1:c.59387A>T (TTN)	XP_024308868.1:p.Asp19796Val