Canonical Allele Identifier: CA349411753

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396913G>A (hg19) ; chr2:g.178532186G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532186G>A , CM000664.2:g.178532186G>A	GRCh38
NC_000002.11:g.179396913G>A , CM000664.1:g.179396913G>A	GRCh37
NC_000002.10:g.179105159G>A	NCBI36
NG_011618.3:g.303617C>T , LRG_391:g.303617C>T
NG_051363.1:g.14360G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96725C>T (TTN)	ENSP00000343764.6:p.Thr32242Ile
ENST00000342175.11:c.77810C>T (TTN)	ENSP00000340554.6:p.Thr25937Ile
ENST00000359218.10:c.77609C>T (TTN)	ENSP00000352154.5:p.Thr25870Ile
ENST00000342175.10:c.77810C>T (TTN)	ENSP00000340554.6:p.Thr25937Ile
ENST00000342992.10:c.96725C>T (TTN)	ENSP00000343764.6:p.Thr32242Ile
ENST00000359218.9:c.77609C>T (TTN)	ENSP00000352154.5:p.Thr25870Ile
ENST00000460472.6:c.77234C>T (TTN)	ENSP00000434586.1:p.Thr25745Ile
ENST00000589042.5:c.104429C>T (TTN) MANE Select	ENSP00000467141.1:p.Thr34810Ile
ENST00000591111.5:c.99506C>T (TTN)	ENSP00000465570.1:p.Thr33169Ile
ENST00000615779.4:c.99506C>T (TTN)	ENSP00000483597.1:p.Thr33169Ile
NM_001256850.1:c.99506C>T (TTN)	NP_001243779.1:p.Thr33169Ile
NM_001267550.2:c.104429C>T (TTN) MANE Select	NP_001254479.2:p.Thr34810Ile
NM_003319.4:c.77234C>T (TTN)	NP_003310.4:p.Thr25745Ile
NM_133378.4:c.96725C>T (TTN)	NP_596869.4:p.Thr32242Ile
NM_133432.3:c.77609C>T (TTN)	NP_597676.3:p.Thr25870Ile
NM_133437.4:c.77810C>T (TTN)	NP_597681.4:p.Thr25937Ile
NR_038271.1:n.446+8550G>A (TTN-AS1)
NR_038272.1:n.220-3546G>A (TTN-AS1)
XM_011511729.1:c.103526C>T (TTN)	XP_011510031.1:p.Thr34509Ile
XM_011511730.1:c.77420C>T (TTN)	XP_011510032.1:p.Thr25807Ile
XM_011511731.1:c.77279C>T (TTN)	XP_011510033.1:p.Thr25760Ile
XM_017004819.1:c.103322C>T (TTN)	XP_016860308.1:p.Thr34441Ile
XM_017004820.1:c.98720C>T (TTN)	XP_016860309.1:p.Thr32907Ile
XM_017004821.1:c.98717C>T (TTN)	XP_016860310.1:p.Thr32906Ile
XM_017004822.1:c.95759C>T (TTN)	XP_016860311.1:p.Thr31920Ile
XM_017004823.1:c.77375C>T (TTN)	XP_016860312.1:p.Thr25792Ile
XM_024453094.1:c.98870C>T (TTN)	XP_024308862.1:p.Thr32957Ile
XM_024453095.1:c.98867C>T (TTN)	XP_024308863.1:p.Thr32956Ile
XM_024453096.1:c.98300C>T (TTN)	XP_024308864.1:p.Thr32767Ile
XM_024453097.1:c.95642C>T (TTN)	XP_024308865.1:p.Thr31881Ile
XM_024453098.1:c.95561C>T (TTN)	XP_024308866.1:p.Thr31854Ile
XM_024453099.1:c.77324C>T (TTN)	XP_024308867.1:p.Thr25775Ile
XM_024453100.1:c.67178C>T (TTN)	XP_024308868.1:p.Thr22393Ile