Canonical Allele Identifier: CA349457321

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409144C>G (hg19) ; chr2:g.178544417C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544417C>G , CM000664.2:g.178544417C>G	GRCh38
NC_000002.11:g.179409144C>G , CM000664.1:g.179409144C>G	GRCh37
NC_000002.10:g.179117390C>G	NCBI36
NG_011618.3:g.291386G>C , LRG_391:g.291386G>C
NG_051363.1:g.26591C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88108G>C (TTN)	ENSP00000343764.6:p.Gly29370Arg
ENST00000342175.11:c.69193G>C (TTN)	ENSP00000340554.6:p.Gly23065Arg
ENST00000359218.10:c.68992G>C (TTN)	ENSP00000352154.5:p.Gly22998Arg
ENST00000342175.10:c.69193G>C (TTN)	ENSP00000340554.6:p.Gly23065Arg
ENST00000342992.10:c.88108G>C (TTN)	ENSP00000343764.6:p.Gly29370Arg
ENST00000359218.9:c.68992G>C (TTN)	ENSP00000352154.5:p.Gly22998Arg
ENST00000460472.6:c.68617G>C (TTN)	ENSP00000434586.1:p.Gly22873Arg
ENST00000589042.5:c.95812G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly31938Arg
ENST00000591111.5:c.90889G>C (TTN)	ENSP00000465570.1:p.Gly30297Arg
ENST00000615779.4:c.90889G>C (TTN)	ENSP00000483597.1:p.Gly30297Arg
NM_001256850.1:c.90889G>C (TTN)	NP_001243779.1:p.Gly30297Arg
NM_001267550.2:c.95812G>C (TTN) MANE Select	NP_001254479.2:p.Gly31938Arg
NM_003319.4:c.68617G>C (TTN)	NP_003310.4:p.Gly22873Arg
NM_133378.4:c.88108G>C (TTN)	NP_596869.4:p.Gly29370Arg
NM_133432.3:c.68992G>C (TTN)	NP_597676.3:p.Gly22998Arg
NM_133437.4:c.69193G>C (TTN)	NP_597681.4:p.Gly23065Arg
NR_038271.1:n.446+20781C>G (TTN-AS1)
NR_038272.1:n.2043+2056C>G (TTN-AS1)
XM_011511729.1:c.94909G>C (TTN)	XP_011510031.1:p.Gly31637Arg
XM_011511730.1:c.68803G>C (TTN)	XP_011510032.1:p.Gly22935Arg
XM_011511731.1:c.68662G>C (TTN)	XP_011510033.1:p.Gly22888Arg
XM_017004819.1:c.94705G>C (TTN)	XP_016860308.1:p.Gly31569Arg
XM_017004820.1:c.90103G>C (TTN)	XP_016860309.1:p.Gly30035Arg
XM_017004821.1:c.90100G>C (TTN)	XP_016860310.1:p.Gly30034Arg
XM_017004822.1:c.87142G>C (TTN)	XP_016860311.1:p.Gly29048Arg
XM_017004823.1:c.68758G>C (TTN)	XP_016860312.1:p.Gly22920Arg
XM_024453094.1:c.90253G>C (TTN)	XP_024308862.1:p.Gly30085Arg
XM_024453095.1:c.90250G>C (TTN)	XP_024308863.1:p.Gly30084Arg
XM_024453096.1:c.89683G>C (TTN)	XP_024308864.1:p.Gly29895Arg
XM_024453097.1:c.87025G>C (TTN)	XP_024308865.1:p.Gly29009Arg
XM_024453098.1:c.86944G>C (TTN)	XP_024308866.1:p.Gly28982Arg
XM_024453099.1:c.68707G>C (TTN)	XP_024308867.1:p.Gly22903Arg
XM_024453100.1:c.58561G>C (TTN)	XP_024308868.1:p.Gly19521Arg