Canonical Allele Identifier: CA349407328

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395374C>T (hg19) ; chr2:g.178530647C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530647C>T , CM000664.2:g.178530647C>T	GRCh38
NC_000002.11:g.179395374C>T , CM000664.1:g.179395374C>T	GRCh37
NC_000002.10:g.179103620C>T	NCBI36
NG_011618.3:g.305156G>A , LRG_391:g.305156G>A
NG_051363.1:g.12821C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98264G>A (TTN)	ENSP00000343764.6:p.Gly32755Asp
ENST00000342175.11:c.79349G>A (TTN)	ENSP00000340554.6:p.Gly26450Asp
ENST00000359218.10:c.79148G>A (TTN)	ENSP00000352154.5:p.Gly26383Asp
ENST00000342175.10:c.79349G>A (TTN)	ENSP00000340554.6:p.Gly26450Asp
ENST00000342992.10:c.98264G>A (TTN)	ENSP00000343764.6:p.Gly32755Asp
ENST00000359218.9:c.79148G>A (TTN)	ENSP00000352154.5:p.Gly26383Asp
ENST00000460472.6:c.78773G>A (TTN)	ENSP00000434586.1:p.Gly26258Asp
ENST00000589042.5:c.105968G>A (TTN) MANE Select	ENSP00000467141.1:p.Gly35323Asp
ENST00000591111.5:c.101045G>A (TTN)	ENSP00000465570.1:p.Gly33682Asp
ENST00000615779.4:c.101045G>A (TTN)	ENSP00000483597.1:p.Gly33682Asp
NM_001256850.1:c.101045G>A (TTN)	NP_001243779.1:p.Gly33682Asp
NM_001267550.2:c.105968G>A (TTN) MANE Select	NP_001254479.2:p.Gly35323Asp
NM_003319.4:c.78773G>A (TTN)	NP_003310.4:p.Gly26258Asp
NM_133378.4:c.98264G>A (TTN)	NP_596869.4:p.Gly32755Asp
NM_133432.3:c.79148G>A (TTN)	NP_597676.3:p.Gly26383Asp
NM_133437.4:c.79349G>A (TTN)	NP_597681.4:p.Gly26450Asp
NR_038271.1:n.446+7011C>T (TTN-AS1)
NR_038272.1:n.220-5085C>T (TTN-AS1)
XM_011511729.1:c.105065G>A (TTN)	XP_011510031.1:p.Gly35022Asp
XM_011511730.1:c.78959G>A (TTN)	XP_011510032.1:p.Gly26320Asp
XM_011511731.1:c.78818G>A (TTN)	XP_011510033.1:p.Gly26273Asp
XM_017004819.1:c.104861G>A (TTN)	XP_016860308.1:p.Gly34954Asp
XM_017004820.1:c.100259G>A (TTN)	XP_016860309.1:p.Gly33420Asp
XM_017004821.1:c.100256G>A (TTN)	XP_016860310.1:p.Gly33419Asp
XM_017004822.1:c.97298G>A (TTN)	XP_016860311.1:p.Gly32433Asp
XM_017004823.1:c.78914G>A (TTN)	XP_016860312.1:p.Gly26305Asp
XM_024453094.1:c.100409G>A (TTN)	XP_024308862.1:p.Gly33470Asp
XM_024453095.1:c.100406G>A (TTN)	XP_024308863.1:p.Gly33469Asp
XM_024453096.1:c.99839G>A (TTN)	XP_024308864.1:p.Gly33280Asp
XM_024453097.1:c.97181G>A (TTN)	XP_024308865.1:p.Gly32394Asp
XM_024453098.1:c.97100G>A (TTN)	XP_024308866.1:p.Gly32367Asp
XM_024453099.1:c.78863G>A (TTN)	XP_024308867.1:p.Gly26288Asp
XM_024453100.1:c.68717G>A (TTN)	XP_024308868.1:p.Gly22906Asp