Canonical Allele Identifier: CA349467461

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179411032T>C (hg19) ; chr2:g.178546305T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546305T>C , CM000664.2:g.178546305T>C	GRCh38
NC_000002.11:g.179411032T>C , CM000664.1:g.179411032T>C	GRCh37
NC_000002.10:g.179119278T>C	NCBI36
NG_011618.3:g.289498A>G , LRG_391:g.289498A>G
NG_051363.1:g.28479T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.87322A>G (TTN)	ENSP00000343764.6:p.Lys29108Glu
ENST00000342175.11:c.68407A>G (TTN)	ENSP00000340554.6:p.Lys22803Glu
ENST00000359218.10:c.68206A>G (TTN)	ENSP00000352154.5:p.Lys22736Glu
ENST00000342175.10:c.68407A>G (TTN)	ENSP00000340554.6:p.Lys22803Glu
ENST00000342992.10:c.87322A>G (TTN)	ENSP00000343764.6:p.Lys29108Glu
ENST00000359218.9:c.68206A>G (TTN)	ENSP00000352154.5:p.Lys22736Glu
ENST00000460472.6:c.67831A>G (TTN)	ENSP00000434586.1:p.Lys22611Glu
ENST00000589042.5:c.95026A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys31676Glu
ENST00000591111.5:c.90103A>G (TTN)	ENSP00000465570.1:p.Lys30035Glu
ENST00000615779.4:c.90103A>G (TTN)	ENSP00000483597.1:p.Lys30035Glu
NM_001256850.1:c.90103A>G (TTN)	NP_001243779.1:p.Lys30035Glu
NM_001267550.2:c.95026A>G (TTN) MANE Select	NP_001254479.2:p.Lys31676Glu
NM_003319.4:c.67831A>G (TTN)	NP_003310.4:p.Lys22611Glu
NM_133378.4:c.87322A>G (TTN)	NP_596869.4:p.Lys29108Glu
NM_133432.3:c.68206A>G (TTN)	NP_597676.3:p.Lys22736Glu
NM_133437.4:c.68407A>G (TTN)	NP_597681.4:p.Lys22803Glu
NR_038271.1:n.446+22669T>C (TTN-AS1)
NR_038272.1:n.2043+3944T>C (TTN-AS1)
XM_011511729.1:c.94123A>G (TTN)	XP_011510031.1:p.Lys31375Glu
XM_011511730.1:c.68017A>G (TTN)	XP_011510032.1:p.Lys22673Glu
XM_011511731.1:c.67876A>G (TTN)	XP_011510033.1:p.Lys22626Glu
XM_017004819.1:c.93919A>G (TTN)	XP_016860308.1:p.Lys31307Glu
XM_017004820.1:c.89317A>G (TTN)	XP_016860309.1:p.Lys29773Glu
XM_017004821.1:c.89314A>G (TTN)	XP_016860310.1:p.Lys29772Glu
XM_017004822.1:c.86356A>G (TTN)	XP_016860311.1:p.Lys28786Glu
XM_017004823.1:c.67972A>G (TTN)	XP_016860312.1:p.Lys22658Glu
XM_024453094.1:c.89467A>G (TTN)	XP_024308862.1:p.Lys29823Glu
XM_024453095.1:c.89464A>G (TTN)	XP_024308863.1:p.Lys29822Glu
XM_024453096.1:c.88897A>G (TTN)	XP_024308864.1:p.Lys29633Glu
XM_024453097.1:c.86239A>G (TTN)	XP_024308865.1:p.Lys28747Glu
XM_024453098.1:c.86158A>G (TTN)	XP_024308866.1:p.Lys28720Glu
XM_024453099.1:c.67921A>G (TTN)	XP_024308867.1:p.Lys22641Glu
XM_024453100.1:c.57775A>G (TTN)	XP_024308868.1:p.Lys19259Glu