Canonical Allele Identifier: CA349406759

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395164T>A (hg19) ; chr2:g.178530437T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530437T>A , CM000664.2:g.178530437T>A	GRCh38
NC_000002.11:g.179395164T>A , CM000664.1:g.179395164T>A	GRCh37
NC_000002.10:g.179103410T>A	NCBI36
NG_011618.3:g.305366A>T , LRG_391:g.305366A>T
NG_051363.1:g.12611T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98474A>T (TTN)	ENSP00000343764.6:p.Lys32825Met
ENST00000342175.11:c.79559A>T (TTN)	ENSP00000340554.6:p.Lys26520Met
ENST00000359218.10:c.79358A>T (TTN)	ENSP00000352154.5:p.Lys26453Met
ENST00000342175.10:c.79559A>T (TTN)	ENSP00000340554.6:p.Lys26520Met
ENST00000342992.10:c.98474A>T (TTN)	ENSP00000343764.6:p.Lys32825Met
ENST00000359218.9:c.79358A>T (TTN)	ENSP00000352154.5:p.Lys26453Met
ENST00000460472.6:c.78983A>T (TTN)	ENSP00000434586.1:p.Lys26328Met
ENST00000589042.5:c.106178A>T (TTN) MANE Select	ENSP00000467141.1:p.Lys35393Met
ENST00000591111.5:c.101255A>T (TTN)	ENSP00000465570.1:p.Lys33752Met
ENST00000615779.4:c.101255A>T (TTN)	ENSP00000483597.1:p.Lys33752Met
NM_001256850.1:c.101255A>T (TTN)	NP_001243779.1:p.Lys33752Met
NM_001267550.2:c.106178A>T (TTN) MANE Select	NP_001254479.2:p.Lys35393Met
NM_003319.4:c.78983A>T (TTN)	NP_003310.4:p.Lys26328Met
NM_133378.4:c.98474A>T (TTN)	NP_596869.4:p.Lys32825Met
NM_133432.3:c.79358A>T (TTN)	NP_597676.3:p.Lys26453Met
NM_133437.4:c.79559A>T (TTN)	NP_597681.4:p.Lys26520Met
NR_038271.1:n.446+6801T>A (TTN-AS1)
NR_038272.1:n.220-5295T>A (TTN-AS1)
XM_011511729.1:c.105275A>T (TTN)	XP_011510031.1:p.Lys35092Met
XM_011511730.1:c.79169A>T (TTN)	XP_011510032.1:p.Lys26390Met
XM_011511731.1:c.79028A>T (TTN)	XP_011510033.1:p.Lys26343Met
XM_017004819.1:c.105071A>T (TTN)	XP_016860308.1:p.Lys35024Met
XM_017004820.1:c.100469A>T (TTN)	XP_016860309.1:p.Lys33490Met
XM_017004821.1:c.100466A>T (TTN)	XP_016860310.1:p.Lys33489Met
XM_017004822.1:c.97508A>T (TTN)	XP_016860311.1:p.Lys32503Met
XM_017004823.1:c.79124A>T (TTN)	XP_016860312.1:p.Lys26375Met
XM_024453094.1:c.100619A>T (TTN)	XP_024308862.1:p.Lys33540Met
XM_024453095.1:c.100616A>T (TTN)	XP_024308863.1:p.Lys33539Met
XM_024453096.1:c.100049A>T (TTN)	XP_024308864.1:p.Lys33350Met
XM_024453097.1:c.97391A>T (TTN)	XP_024308865.1:p.Lys32464Met
XM_024453098.1:c.97310A>T (TTN)	XP_024308866.1:p.Lys32437Met
XM_024453099.1:c.79073A>T (TTN)	XP_024308867.1:p.Lys26358Met
XM_024453100.1:c.68927A>T (TTN)	XP_024308868.1:p.Lys22976Met