Canonical Allele Identifier: CA349406822

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395175T>C (hg19) ; chr2:g.178530448T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530448T>C , CM000664.2:g.178530448T>C	GRCh38
NC_000002.11:g.179395175T>C , CM000664.1:g.179395175T>C	GRCh37
NC_000002.10:g.179103421T>C	NCBI36
NG_011618.3:g.305355A>G , LRG_391:g.305355A>G
NG_051363.1:g.12622T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98463A>G (TTN)	ENSP00000343764.6:p.Ile32821Met
ENST00000342175.11:c.79548A>G (TTN)	ENSP00000340554.6:p.Ile26516Met
ENST00000359218.10:c.79347A>G (TTN)	ENSP00000352154.5:p.Ile26449Met
ENST00000342175.10:c.79548A>G (TTN)	ENSP00000340554.6:p.Ile26516Met
ENST00000342992.10:c.98463A>G (TTN)	ENSP00000343764.6:p.Ile32821Met
ENST00000359218.9:c.79347A>G (TTN)	ENSP00000352154.5:p.Ile26449Met
ENST00000460472.6:c.78972A>G (TTN)	ENSP00000434586.1:p.Ile26324Met
ENST00000589042.5:c.106167A>G (TTN) MANE Select	ENSP00000467141.1:p.Ile35389Met
ENST00000591111.5:c.101244A>G (TTN)	ENSP00000465570.1:p.Ile33748Met
ENST00000615779.4:c.101244A>G (TTN)	ENSP00000483597.1:p.Ile33748Met
NM_001256850.1:c.101244A>G (TTN)	NP_001243779.1:p.Ile33748Met
NM_001267550.2:c.106167A>G (TTN) MANE Select	NP_001254479.2:p.Ile35389Met
NM_003319.4:c.78972A>G (TTN)	NP_003310.4:p.Ile26324Met
NM_133378.4:c.98463A>G (TTN)	NP_596869.4:p.Ile32821Met
NM_133432.3:c.79347A>G (TTN)	NP_597676.3:p.Ile26449Met
NM_133437.4:c.79548A>G (TTN)	NP_597681.4:p.Ile26516Met
NR_038271.1:n.446+6812T>C (TTN-AS1)
NR_038272.1:n.220-5284T>C (TTN-AS1)
XM_011511729.1:c.105264A>G (TTN)	XP_011510031.1:p.Ile35088Met
XM_011511730.1:c.79158A>G (TTN)	XP_011510032.1:p.Ile26386Met
XM_011511731.1:c.79017A>G (TTN)	XP_011510033.1:p.Ile26339Met
XM_017004819.1:c.105060A>G (TTN)	XP_016860308.1:p.Ile35020Met
XM_017004820.1:c.100458A>G (TTN)	XP_016860309.1:p.Ile33486Met
XM_017004821.1:c.100455A>G (TTN)	XP_016860310.1:p.Ile33485Met
XM_017004822.1:c.97497A>G (TTN)	XP_016860311.1:p.Ile32499Met
XM_017004823.1:c.79113A>G (TTN)	XP_016860312.1:p.Ile26371Met
XM_024453094.1:c.100608A>G (TTN)	XP_024308862.1:p.Ile33536Met
XM_024453095.1:c.100605A>G (TTN)	XP_024308863.1:p.Ile33535Met
XM_024453096.1:c.100038A>G (TTN)	XP_024308864.1:p.Ile33346Met
XM_024453097.1:c.97380A>G (TTN)	XP_024308865.1:p.Ile32460Met
XM_024453098.1:c.97299A>G (TTN)	XP_024308866.1:p.Ile32433Met
XM_024453099.1:c.79062A>G (TTN)	XP_024308867.1:p.Ile26354Met
XM_024453100.1:c.68916A>G (TTN)	XP_024308868.1:p.Ile22972Met