Canonical Allele Identifier: CA349407329

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395375C>A (hg19) ; chr2:g.178530648C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530648C>A , CM000664.2:g.178530648C>A	GRCh38
NC_000002.11:g.179395375C>A , CM000664.1:g.179395375C>A	GRCh37
NC_000002.10:g.179103621C>A	NCBI36
NG_011618.3:g.305155G>T , LRG_391:g.305155G>T
NG_051363.1:g.12822C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98263G>T (TTN)	ENSP00000343764.6:p.Gly32755Cys
ENST00000342175.11:c.79348G>T (TTN)	ENSP00000340554.6:p.Gly26450Cys
ENST00000359218.10:c.79147G>T (TTN)	ENSP00000352154.5:p.Gly26383Cys
ENST00000342175.10:c.79348G>T (TTN)	ENSP00000340554.6:p.Gly26450Cys
ENST00000342992.10:c.98263G>T (TTN)	ENSP00000343764.6:p.Gly32755Cys
ENST00000359218.9:c.79147G>T (TTN)	ENSP00000352154.5:p.Gly26383Cys
ENST00000460472.6:c.78772G>T (TTN)	ENSP00000434586.1:p.Gly26258Cys
ENST00000589042.5:c.105967G>T (TTN) MANE Select	ENSP00000467141.1:p.Gly35323Cys
ENST00000591111.5:c.101044G>T (TTN)	ENSP00000465570.1:p.Gly33682Cys
ENST00000615779.4:c.101044G>T (TTN)	ENSP00000483597.1:p.Gly33682Cys
NM_001256850.1:c.101044G>T (TTN)	NP_001243779.1:p.Gly33682Cys
NM_001267550.2:c.105967G>T (TTN) MANE Select	NP_001254479.2:p.Gly35323Cys
NM_003319.4:c.78772G>T (TTN)	NP_003310.4:p.Gly26258Cys
NM_133378.4:c.98263G>T (TTN)	NP_596869.4:p.Gly32755Cys
NM_133432.3:c.79147G>T (TTN)	NP_597676.3:p.Gly26383Cys
NM_133437.4:c.79348G>T (TTN)	NP_597681.4:p.Gly26450Cys
NR_038271.1:n.446+7012C>A (TTN-AS1)
NR_038272.1:n.220-5084C>A (TTN-AS1)
XM_011511729.1:c.105064G>T (TTN)	XP_011510031.1:p.Gly35022Cys
XM_011511730.1:c.78958G>T (TTN)	XP_011510032.1:p.Gly26320Cys
XM_011511731.1:c.78817G>T (TTN)	XP_011510033.1:p.Gly26273Cys
XM_017004819.1:c.104860G>T (TTN)	XP_016860308.1:p.Gly34954Cys
XM_017004820.1:c.100258G>T (TTN)	XP_016860309.1:p.Gly33420Cys
XM_017004821.1:c.100255G>T (TTN)	XP_016860310.1:p.Gly33419Cys
XM_017004822.1:c.97297G>T (TTN)	XP_016860311.1:p.Gly32433Cys
XM_017004823.1:c.78913G>T (TTN)	XP_016860312.1:p.Gly26305Cys
XM_024453094.1:c.100408G>T (TTN)	XP_024308862.1:p.Gly33470Cys
XM_024453095.1:c.100405G>T (TTN)	XP_024308863.1:p.Gly33469Cys
XM_024453096.1:c.99838G>T (TTN)	XP_024308864.1:p.Gly33280Cys
XM_024453097.1:c.97180G>T (TTN)	XP_024308865.1:p.Gly32394Cys
XM_024453098.1:c.97099G>T (TTN)	XP_024308866.1:p.Gly32367Cys
XM_024453099.1:c.78862G>T (TTN)	XP_024308867.1:p.Gly26288Cys
XM_024453100.1:c.68716G>T (TTN)	XP_024308868.1:p.Gly22906Cys