Canonical Allele Identifier: CA349483593

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179455842C>T (hg19) ; chr2:g.178591115C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591115C>T , CM000664.2:g.178591115C>T	GRCh38
NC_000002.11:g.179455842C>T , CM000664.1:g.179455842C>T	GRCh37
NC_000002.10:g.179164088C>T	NCBI36
NG_011618.3:g.244688G>A , LRG_391:g.244688G>A
NG_051363.1:g.73289C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52906G>A (TTN)	ENSP00000343764.6:p.Val17636Met
ENST00000342175.11:c.33991G>A (TTN)	ENSP00000340554.6:p.Val11331Met
ENST00000359218.10:c.33790G>A (TTN)	ENSP00000352154.5:p.Val11264Met
ENST00000342175.10:c.33991G>A (TTN)	ENSP00000340554.6:p.Val11331Met
ENST00000342992.10:c.52906G>A (TTN)	ENSP00000343764.6:p.Val17636Met
ENST00000359218.9:c.33790G>A (TTN)	ENSP00000352154.5:p.Val11264Met
ENST00000460472.6:c.33415G>A (TTN)	ENSP00000434586.1:p.Val11139Met
ENST00000589042.5:c.60610G>A (TTN) MANE Select	ENSP00000467141.1:p.Val20204Met
ENST00000591111.5:c.55687G>A (TTN)	ENSP00000465570.1:p.Val18563Met
ENST00000615779.4:c.55687G>A (TTN)	ENSP00000483597.1:p.Val18563Met
NM_001256850.1:c.55687G>A (TTN)	NP_001243779.1:p.Val18563Met
NM_001267550.2:c.60610G>A (TTN) MANE Select	NP_001254479.2:p.Val20204Met
NM_003319.4:c.33415G>A (TTN)	NP_003310.4:p.Val11139Met
NM_133378.4:c.52906G>A (TTN)	NP_596869.4:p.Val17636Met
NM_133432.3:c.33790G>A (TTN)	NP_597676.3:p.Val11264Met
NM_133437.4:c.33991G>A (TTN)	NP_597681.4:p.Val11331Met
NR_038271.1:n.597-6481C>T (TTN-AS1)
NR_038272.1:n.3189-24C>T (TTN-AS1)
XM_011511729.1:c.59707G>A (TTN)	XP_011510031.1:p.Val19903Met
XM_011511730.1:c.33601G>A (TTN)	XP_011510032.1:p.Val11201Met
XM_011511731.1:c.33460G>A (TTN)	XP_011510033.1:p.Val11154Met
XM_017004819.1:c.59503G>A (TTN)	XP_016860308.1:p.Val19835Met
XM_017004820.1:c.54901G>A (TTN)	XP_016860309.1:p.Val18301Met
XM_017004821.1:c.54898G>A (TTN)	XP_016860310.1:p.Val18300Met
XM_017004822.1:c.51940G>A (TTN)	XP_016860311.1:p.Val17314Met
XM_017004823.1:c.33556G>A (TTN)	XP_016860312.1:p.Val11186Met
XM_024453094.1:c.55051G>A (TTN)	XP_024308862.1:p.Val18351Met
XM_024453095.1:c.55048G>A (TTN)	XP_024308863.1:p.Val18350Met
XM_024453096.1:c.54481G>A (TTN)	XP_024308864.1:p.Val18161Met
XM_024453097.1:c.51823G>A (TTN)	XP_024308865.1:p.Val17275Met
XM_024453098.1:c.51742G>A (TTN)	XP_024308866.1:p.Val17248Met
XM_024453099.1:c.33505G>A (TTN)	XP_024308867.1:p.Val11169Met
XM_024453100.1:c.23359G>A (TTN)	XP_024308868.1:p.Val7787Met