Canonical Allele Identifier: CA349405955

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394993G>T (hg19) ; chr2:g.178530266G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530266G>T , CM000664.2:g.178530266G>T	GRCh38
NC_000002.11:g.179394993G>T , CM000664.1:g.179394993G>T	GRCh37
NC_000002.10:g.179103239G>T	NCBI36
NG_011618.3:g.305537C>A , LRG_391:g.305537C>A
NG_051363.1:g.12440G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98645C>A (TTN)	ENSP00000343764.6:p.Thr32882Asn
ENST00000342175.11:c.79730C>A (TTN)	ENSP00000340554.6:p.Thr26577Asn
ENST00000359218.10:c.79529C>A (TTN)	ENSP00000352154.5:p.Thr26510Asn
ENST00000342175.10:c.79730C>A (TTN)	ENSP00000340554.6:p.Thr26577Asn
ENST00000342992.10:c.98645C>A (TTN)	ENSP00000343764.6:p.Thr32882Asn
ENST00000359218.9:c.79529C>A (TTN)	ENSP00000352154.5:p.Thr26510Asn
ENST00000460472.6:c.79154C>A (TTN)	ENSP00000434586.1:p.Thr26385Asn
ENST00000589042.5:c.106349C>A (TTN) MANE Select	ENSP00000467141.1:p.Thr35450Asn
ENST00000591111.5:c.101426C>A (TTN)	ENSP00000465570.1:p.Thr33809Asn
ENST00000615779.4:c.101426C>A (TTN)	ENSP00000483597.1:p.Thr33809Asn
NM_001256850.1:c.101426C>A (TTN)	NP_001243779.1:p.Thr33809Asn
NM_001267550.2:c.106349C>A (TTN) MANE Select	NP_001254479.2:p.Thr35450Asn
NM_003319.4:c.79154C>A (TTN)	NP_003310.4:p.Thr26385Asn
NM_133378.4:c.98645C>A (TTN)	NP_596869.4:p.Thr32882Asn
NM_133432.3:c.79529C>A (TTN)	NP_597676.3:p.Thr26510Asn
NM_133437.4:c.79730C>A (TTN)	NP_597681.4:p.Thr26577Asn
NR_038271.1:n.446+6630G>T (TTN-AS1)
NR_038272.1:n.220-5466G>T (TTN-AS1)
XM_011511729.1:c.105446C>A (TTN)	XP_011510031.1:p.Thr35149Asn
XM_011511730.1:c.79340C>A (TTN)	XP_011510032.1:p.Thr26447Asn
XM_011511731.1:c.79199C>A (TTN)	XP_011510033.1:p.Thr26400Asn
XM_017004819.1:c.105242C>A (TTN)	XP_016860308.1:p.Thr35081Asn
XM_017004820.1:c.100640C>A (TTN)	XP_016860309.1:p.Thr33547Asn
XM_017004821.1:c.100637C>A (TTN)	XP_016860310.1:p.Thr33546Asn
XM_017004822.1:c.97679C>A (TTN)	XP_016860311.1:p.Thr32560Asn
XM_017004823.1:c.79295C>A (TTN)	XP_016860312.1:p.Thr26432Asn
XM_024453094.1:c.100790C>A (TTN)	XP_024308862.1:p.Thr33597Asn
XM_024453095.1:c.100787C>A (TTN)	XP_024308863.1:p.Thr33596Asn
XM_024453096.1:c.100220C>A (TTN)	XP_024308864.1:p.Thr33407Asn
XM_024453097.1:c.97562C>A (TTN)	XP_024308865.1:p.Thr32521Asn
XM_024453098.1:c.97481C>A (TTN)	XP_024308866.1:p.Thr32494Asn
XM_024453099.1:c.79244C>A (TTN)	XP_024308867.1:p.Thr26415Asn
XM_024453100.1:c.69098C>A (TTN)	XP_024308868.1:p.Thr23033Asn