Canonical Allele Identifier: CA349407321

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395371T>C (hg19) ; chr2:g.178530644T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530644T>C , CM000664.2:g.178530644T>C	GRCh38
NC_000002.11:g.179395371T>C , CM000664.1:g.179395371T>C	GRCh37
NC_000002.10:g.179103617T>C	NCBI36
NG_011618.3:g.305159A>G , LRG_391:g.305159A>G
NG_051363.1:g.12818T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98267A>G (TTN)	ENSP00000343764.6:p.Lys32756Arg
ENST00000342175.11:c.79352A>G (TTN)	ENSP00000340554.6:p.Lys26451Arg
ENST00000359218.10:c.79151A>G (TTN)	ENSP00000352154.5:p.Lys26384Arg
ENST00000342175.10:c.79352A>G (TTN)	ENSP00000340554.6:p.Lys26451Arg
ENST00000342992.10:c.98267A>G (TTN)	ENSP00000343764.6:p.Lys32756Arg
ENST00000359218.9:c.79151A>G (TTN)	ENSP00000352154.5:p.Lys26384Arg
ENST00000460472.6:c.78776A>G (TTN)	ENSP00000434586.1:p.Lys26259Arg
ENST00000589042.5:c.105971A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys35324Arg
ENST00000591111.5:c.101048A>G (TTN)	ENSP00000465570.1:p.Lys33683Arg
ENST00000615779.4:c.101048A>G (TTN)	ENSP00000483597.1:p.Lys33683Arg
NM_001256850.1:c.101048A>G (TTN)	NP_001243779.1:p.Lys33683Arg
NM_001267550.2:c.105971A>G (TTN) MANE Select	NP_001254479.2:p.Lys35324Arg
NM_003319.4:c.78776A>G (TTN)	NP_003310.4:p.Lys26259Arg
NM_133378.4:c.98267A>G (TTN)	NP_596869.4:p.Lys32756Arg
NM_133432.3:c.79151A>G (TTN)	NP_597676.3:p.Lys26384Arg
NM_133437.4:c.79352A>G (TTN)	NP_597681.4:p.Lys26451Arg
NR_038271.1:n.446+7008T>C (TTN-AS1)
NR_038272.1:n.220-5088T>C (TTN-AS1)
XM_011511729.1:c.105068A>G (TTN)	XP_011510031.1:p.Lys35023Arg
XM_011511730.1:c.78962A>G (TTN)	XP_011510032.1:p.Lys26321Arg
XM_011511731.1:c.78821A>G (TTN)	XP_011510033.1:p.Lys26274Arg
XM_017004819.1:c.104864A>G (TTN)	XP_016860308.1:p.Lys34955Arg
XM_017004820.1:c.100262A>G (TTN)	XP_016860309.1:p.Lys33421Arg
XM_017004821.1:c.100259A>G (TTN)	XP_016860310.1:p.Lys33420Arg
XM_017004822.1:c.97301A>G (TTN)	XP_016860311.1:p.Lys32434Arg
XM_017004823.1:c.78917A>G (TTN)	XP_016860312.1:p.Lys26306Arg
XM_024453094.1:c.100412A>G (TTN)	XP_024308862.1:p.Lys33471Arg
XM_024453095.1:c.100409A>G (TTN)	XP_024308863.1:p.Lys33470Arg
XM_024453096.1:c.99842A>G (TTN)	XP_024308864.1:p.Lys33281Arg
XM_024453097.1:c.97184A>G (TTN)	XP_024308865.1:p.Lys32395Arg
XM_024453098.1:c.97103A>G (TTN)	XP_024308866.1:p.Lys32368Arg
XM_024453099.1:c.78866A>G (TTN)	XP_024308867.1:p.Lys26289Arg
XM_024453100.1:c.68720A>G (TTN)	XP_024308868.1:p.Lys22907Arg