Canonical Allele Identifier: CA349512577

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179417382A>C (hg19) ; chr2:g.178552655A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178552655A>C , CM000664.2:g.178552655A>C	GRCh38
NC_000002.11:g.179417382A>C , CM000664.1:g.179417382A>C	GRCh37
NC_000002.10:g.179125628A>C	NCBI36
NG_011618.3:g.283148T>G , LRG_391:g.283148T>G
NG_051363.1:g.34829A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.82541T>G (TTN)	ENSP00000343764.6:p.Ile27514Arg
ENST00000342175.11:c.63626T>G (TTN)	ENSP00000340554.6:p.Ile21209Arg
ENST00000359218.10:c.63425T>G (TTN)	ENSP00000352154.5:p.Ile21142Arg
ENST00000342175.10:c.63626T>G (TTN)	ENSP00000340554.6:p.Ile21209Arg
ENST00000342992.10:c.82541T>G (TTN)	ENSP00000343764.6:p.Ile27514Arg
ENST00000359218.9:c.63425T>G (TTN)	ENSP00000352154.5:p.Ile21142Arg
ENST00000460472.6:c.63050T>G (TTN)	ENSP00000434586.1:p.Ile21017Arg
ENST00000589042.5:c.90245T>G (TTN) MANE Select	ENSP00000467141.1:p.Ile30082Arg
ENST00000591111.5:c.85322T>G (TTN)	ENSP00000465570.1:p.Ile28441Arg
ENST00000615779.4:c.85322T>G (TTN)	ENSP00000483597.1:p.Ile28441Arg
NM_001256850.1:c.85322T>G (TTN)	NP_001243779.1:p.Ile28441Arg
NM_001267550.2:c.90245T>G (TTN) MANE Select	NP_001254479.2:p.Ile30082Arg
NM_003319.4:c.63050T>G (TTN)	NP_003310.4:p.Ile21017Arg
NM_133378.4:c.82541T>G (TTN)	NP_596869.4:p.Ile27514Arg
NM_133432.3:c.63425T>G (TTN)	NP_597676.3:p.Ile21142Arg
NM_133437.4:c.63626T>G (TTN)	NP_597681.4:p.Ile21209Arg
NR_038271.1:n.447-18645A>C (TTN-AS1)
NR_038272.1:n.2043+10294A>C (TTN-AS1)
XM_011511729.1:c.89342T>G (TTN)	XP_011510031.1:p.Ile29781Arg
XM_011511730.1:c.63236T>G (TTN)	XP_011510032.1:p.Ile21079Arg
XM_011511731.1:c.63095T>G (TTN)	XP_011510033.1:p.Ile21032Arg
XM_017004819.1:c.89138T>G (TTN)	XP_016860308.1:p.Ile29713Arg
XM_017004820.1:c.84536T>G (TTN)	XP_016860309.1:p.Ile28179Arg
XM_017004821.1:c.84533T>G (TTN)	XP_016860310.1:p.Ile28178Arg
XM_017004822.1:c.81575T>G (TTN)	XP_016860311.1:p.Ile27192Arg
XM_017004823.1:c.63191T>G (TTN)	XP_016860312.1:p.Ile21064Arg
XM_024453094.1:c.84686T>G (TTN)	XP_024308862.1:p.Ile28229Arg
XM_024453095.1:c.84683T>G (TTN)	XP_024308863.1:p.Ile28228Arg
XM_024453096.1:c.84116T>G (TTN)	XP_024308864.1:p.Ile28039Arg
XM_024453097.1:c.81458T>G (TTN)	XP_024308865.1:p.Ile27153Arg
XM_024453098.1:c.81377T>G (TTN)	XP_024308866.1:p.Ile27126Arg
XM_024453099.1:c.63140T>G (TTN)	XP_024308867.1:p.Ile21047Arg
XM_024453100.1:c.52994T>G (TTN)	XP_024308868.1:p.Ile17665Arg