Canonical Allele Identifier: CA349511660

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179417287G>T (hg19) ; chr2:g.178552560G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178552560G>T , CM000664.2:g.178552560G>T	GRCh38
NC_000002.11:g.179417287G>T , CM000664.1:g.179417287G>T	GRCh37
NC_000002.10:g.179125533G>T	NCBI36
NG_011618.3:g.283243C>A , LRG_391:g.283243C>A
NG_051363.1:g.34734G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.82636C>A (TTN)	ENSP00000343764.6:p.Pro27546Thr
ENST00000342175.11:c.63721C>A (TTN)	ENSP00000340554.6:p.Pro21241Thr
ENST00000359218.10:c.63520C>A (TTN)	ENSP00000352154.5:p.Pro21174Thr
ENST00000342175.10:c.63721C>A (TTN)	ENSP00000340554.6:p.Pro21241Thr
ENST00000342992.10:c.82636C>A (TTN)	ENSP00000343764.6:p.Pro27546Thr
ENST00000359218.9:c.63520C>A (TTN)	ENSP00000352154.5:p.Pro21174Thr
ENST00000460472.6:c.63145C>A (TTN)	ENSP00000434586.1:p.Pro21049Thr
ENST00000589042.5:c.90340C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro30114Thr
ENST00000591111.5:c.85417C>A (TTN)	ENSP00000465570.1:p.Pro28473Thr
ENST00000615779.4:c.85417C>A (TTN)	ENSP00000483597.1:p.Pro28473Thr
NM_001256850.1:c.85417C>A (TTN)	NP_001243779.1:p.Pro28473Thr
NM_001267550.2:c.90340C>A (TTN) MANE Select	NP_001254479.2:p.Pro30114Thr
NM_003319.4:c.63145C>A (TTN)	NP_003310.4:p.Pro21049Thr
NM_133378.4:c.82636C>A (TTN)	NP_596869.4:p.Pro27546Thr
NM_133432.3:c.63520C>A (TTN)	NP_597676.3:p.Pro21174Thr
NM_133437.4:c.63721C>A (TTN)	NP_597681.4:p.Pro21241Thr
NR_038271.1:n.447-18740G>T (TTN-AS1)
NR_038272.1:n.2043+10199G>T (TTN-AS1)
XM_011511729.1:c.89437C>A (TTN)	XP_011510031.1:p.Pro29813Thr
XM_011511730.1:c.63331C>A (TTN)	XP_011510032.1:p.Pro21111Thr
XM_011511731.1:c.63190C>A (TTN)	XP_011510033.1:p.Pro21064Thr
XM_017004819.1:c.89233C>A (TTN)	XP_016860308.1:p.Pro29745Thr
XM_017004820.1:c.84631C>A (TTN)	XP_016860309.1:p.Pro28211Thr
XM_017004821.1:c.84628C>A (TTN)	XP_016860310.1:p.Pro28210Thr
XM_017004822.1:c.81670C>A (TTN)	XP_016860311.1:p.Pro27224Thr
XM_017004823.1:c.63286C>A (TTN)	XP_016860312.1:p.Pro21096Thr
XM_024453094.1:c.84781C>A (TTN)	XP_024308862.1:p.Pro28261Thr
XM_024453095.1:c.84778C>A (TTN)	XP_024308863.1:p.Pro28260Thr
XM_024453096.1:c.84211C>A (TTN)	XP_024308864.1:p.Pro28071Thr
XM_024453097.1:c.81553C>A (TTN)	XP_024308865.1:p.Pro27185Thr
XM_024453098.1:c.81472C>A (TTN)	XP_024308866.1:p.Pro27158Thr
XM_024453099.1:c.63235C>A (TTN)	XP_024308867.1:p.Pro21079Thr
XM_024453100.1:c.53089C>A (TTN)	XP_024308868.1:p.Pro17697Thr