Canonical Allele Identifier: CA349411363

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396758G>T (hg19) ; chr2:g.178532031G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532031G>T , CM000664.2:g.178532031G>T	GRCh38
NC_000002.11:g.179396758G>T , CM000664.1:g.179396758G>T	GRCh37
NC_000002.10:g.179105004G>T	NCBI36
NG_011618.3:g.303772C>A , LRG_391:g.303772C>A
NG_051363.1:g.14205G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96880C>A (TTN)	ENSP00000343764.6:p.Pro32294Thr
ENST00000342175.11:c.77965C>A (TTN)	ENSP00000340554.6:p.Pro25989Thr
ENST00000359218.10:c.77764C>A (TTN)	ENSP00000352154.5:p.Pro25922Thr
ENST00000342175.10:c.77965C>A (TTN)	ENSP00000340554.6:p.Pro25989Thr
ENST00000342992.10:c.96880C>A (TTN)	ENSP00000343764.6:p.Pro32294Thr
ENST00000359218.9:c.77764C>A (TTN)	ENSP00000352154.5:p.Pro25922Thr
ENST00000460472.6:c.77389C>A (TTN)	ENSP00000434586.1:p.Pro25797Thr
ENST00000589042.5:c.104584C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro34862Thr
ENST00000591111.5:c.99661C>A (TTN)	ENSP00000465570.1:p.Pro33221Thr
ENST00000615779.4:c.99661C>A (TTN)	ENSP00000483597.1:p.Pro33221Thr
NM_001256850.1:c.99661C>A (TTN)	NP_001243779.1:p.Pro33221Thr
NM_001267550.2:c.104584C>A (TTN) MANE Select	NP_001254479.2:p.Pro34862Thr
NM_003319.4:c.77389C>A (TTN)	NP_003310.4:p.Pro25797Thr
NM_133378.4:c.96880C>A (TTN)	NP_596869.4:p.Pro32294Thr
NM_133432.3:c.77764C>A (TTN)	NP_597676.3:p.Pro25922Thr
NM_133437.4:c.77965C>A (TTN)	NP_597681.4:p.Pro25989Thr
NR_038271.1:n.446+8395G>T (TTN-AS1)
NR_038272.1:n.220-3701G>T (TTN-AS1)
XM_011511729.1:c.103681C>A (TTN)	XP_011510031.1:p.Pro34561Thr
XM_011511730.1:c.77575C>A (TTN)	XP_011510032.1:p.Pro25859Thr
XM_011511731.1:c.77434C>A (TTN)	XP_011510033.1:p.Pro25812Thr
XM_017004819.1:c.103477C>A (TTN)	XP_016860308.1:p.Pro34493Thr
XM_017004820.1:c.98875C>A (TTN)	XP_016860309.1:p.Pro32959Thr
XM_017004821.1:c.98872C>A (TTN)	XP_016860310.1:p.Pro32958Thr
XM_017004822.1:c.95914C>A (TTN)	XP_016860311.1:p.Pro31972Thr
XM_017004823.1:c.77530C>A (TTN)	XP_016860312.1:p.Pro25844Thr
XM_024453094.1:c.99025C>A (TTN)	XP_024308862.1:p.Pro33009Thr
XM_024453095.1:c.99022C>A (TTN)	XP_024308863.1:p.Pro33008Thr
XM_024453096.1:c.98455C>A (TTN)	XP_024308864.1:p.Pro32819Thr
XM_024453097.1:c.95797C>A (TTN)	XP_024308865.1:p.Pro31933Thr
XM_024453098.1:c.95716C>A (TTN)	XP_024308866.1:p.Pro31906Thr
XM_024453099.1:c.77479C>A (TTN)	XP_024308867.1:p.Pro25827Thr
XM_024453100.1:c.67333C>A (TTN)	XP_024308868.1:p.Pro22445Thr