Canonical Allele Identifier: CA349405961

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394994T>G (hg19) ; chr2:g.178530267T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530267T>G , CM000664.2:g.178530267T>G	GRCh38
NC_000002.11:g.179394994T>G , CM000664.1:g.179394994T>G	GRCh37
NC_000002.10:g.179103240T>G	NCBI36
NG_011618.3:g.305536A>C , LRG_391:g.305536A>C
NG_051363.1:g.12441T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98644A>C (TTN)	ENSP00000343764.6:p.Thr32882Pro
ENST00000342175.11:c.79729A>C (TTN)	ENSP00000340554.6:p.Thr26577Pro
ENST00000359218.10:c.79528A>C (TTN)	ENSP00000352154.5:p.Thr26510Pro
ENST00000342175.10:c.79729A>C (TTN)	ENSP00000340554.6:p.Thr26577Pro
ENST00000342992.10:c.98644A>C (TTN)	ENSP00000343764.6:p.Thr32882Pro
ENST00000359218.9:c.79528A>C (TTN)	ENSP00000352154.5:p.Thr26510Pro
ENST00000460472.6:c.79153A>C (TTN)	ENSP00000434586.1:p.Thr26385Pro
ENST00000589042.5:c.106348A>C (TTN) MANE Select	ENSP00000467141.1:p.Thr35450Pro
ENST00000591111.5:c.101425A>C (TTN)	ENSP00000465570.1:p.Thr33809Pro
ENST00000615779.4:c.101425A>C (TTN)	ENSP00000483597.1:p.Thr33809Pro
NM_001256850.1:c.101425A>C (TTN)	NP_001243779.1:p.Thr33809Pro
NM_001267550.2:c.106348A>C (TTN) MANE Select	NP_001254479.2:p.Thr35450Pro
NM_003319.4:c.79153A>C (TTN)	NP_003310.4:p.Thr26385Pro
NM_133378.4:c.98644A>C (TTN)	NP_596869.4:p.Thr32882Pro
NM_133432.3:c.79528A>C (TTN)	NP_597676.3:p.Thr26510Pro
NM_133437.4:c.79729A>C (TTN)	NP_597681.4:p.Thr26577Pro
NR_038271.1:n.446+6631T>G (TTN-AS1)
NR_038272.1:n.220-5465T>G (TTN-AS1)
XM_011511729.1:c.105445A>C (TTN)	XP_011510031.1:p.Thr35149Pro
XM_011511730.1:c.79339A>C (TTN)	XP_011510032.1:p.Thr26447Pro
XM_011511731.1:c.79198A>C (TTN)	XP_011510033.1:p.Thr26400Pro
XM_017004819.1:c.105241A>C (TTN)	XP_016860308.1:p.Thr35081Pro
XM_017004820.1:c.100639A>C (TTN)	XP_016860309.1:p.Thr33547Pro
XM_017004821.1:c.100636A>C (TTN)	XP_016860310.1:p.Thr33546Pro
XM_017004822.1:c.97678A>C (TTN)	XP_016860311.1:p.Thr32560Pro
XM_017004823.1:c.79294A>C (TTN)	XP_016860312.1:p.Thr26432Pro
XM_024453094.1:c.100789A>C (TTN)	XP_024308862.1:p.Thr33597Pro
XM_024453095.1:c.100786A>C (TTN)	XP_024308863.1:p.Thr33596Pro
XM_024453096.1:c.100219A>C (TTN)	XP_024308864.1:p.Thr33407Pro
XM_024453097.1:c.97561A>C (TTN)	XP_024308865.1:p.Thr32521Pro
XM_024453098.1:c.97480A>C (TTN)	XP_024308866.1:p.Thr32494Pro
XM_024453099.1:c.79243A>C (TTN)	XP_024308867.1:p.Thr26415Pro
XM_024453100.1:c.69097A>C (TTN)	XP_024308868.1:p.Thr23033Pro