Canonical Allele Identifier: CA430235327

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395148T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530421T>C , CM000664.2:g.178530421T>C	GRCh38
NC_000002.11:g.179395148T>C , CM000664.1:g.179395148T>C	GRCh37
NC_000002.10:g.179103394T>C	NCBI36
NG_011618.3:g.305382A>G , LRG_391:g.305382A>G
NG_051363.1:g.12595T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98490A>G (TTN)	ENSP00000343764.6:p.Lys32830=
ENST00000342175.11:c.79575A>G (TTN)	ENSP00000340554.6:p.Lys26525=
ENST00000359218.10:c.79374A>G (TTN)	ENSP00000352154.5:p.Lys26458=
ENST00000342175.10:c.79575A>G (TTN)	ENSP00000340554.6:p.Lys26525=
ENST00000342992.10:c.98490A>G (TTN)	ENSP00000343764.6:p.Lys32830=
ENST00000359218.9:c.79374A>G (TTN)	ENSP00000352154.5:p.Lys26458=
ENST00000460472.6:c.78999A>G (TTN)	ENSP00000434586.1:p.Lys26333=
ENST00000589042.5:c.106194A>G (TTN) MANE Select	ENSP00000467141.1:p.Lys35398=
ENST00000591111.5:c.101271A>G (TTN)	ENSP00000465570.1:p.Lys33757=
ENST00000615779.4:c.101271A>G (TTN)	ENSP00000483597.1:p.Lys33757=
NM_001256850.1:c.101271A>G (TTN)	NP_001243779.1:p.Lys33757=
NM_001267550.2:c.106194A>G (TTN) MANE Select	NP_001254479.2:p.Lys35398=
NM_003319.4:c.78999A>G (TTN)	NP_003310.4:p.Lys26333=
NM_133378.4:c.98490A>G (TTN)	NP_596869.4:p.Lys32830=
NM_133432.3:c.79374A>G (TTN)	NP_597676.3:p.Lys26458=
NM_133437.4:c.79575A>G (TTN)	NP_597681.4:p.Lys26525=
NR_038271.1:n.446+6785T>C (TTN-AS1)
NR_038272.1:n.220-5311T>C (TTN-AS1)
XM_011511729.1:c.105291A>G (TTN)	XP_011510031.1:p.Lys35097=
XM_011511730.1:c.79185A>G (TTN)	XP_011510032.1:p.Lys26395=
XM_011511731.1:c.79044A>G (TTN)	XP_011510033.1:p.Lys26348=
XM_017004819.1:c.105087A>G (TTN)	XP_016860308.1:p.Lys35029=
XM_017004820.1:c.100485A>G (TTN)	XP_016860309.1:p.Lys33495=
XM_017004821.1:c.100482A>G (TTN)	XP_016860310.1:p.Lys33494=
XM_017004822.1:c.97524A>G (TTN)	XP_016860311.1:p.Lys32508=
XM_017004823.1:c.79140A>G (TTN)	XP_016860312.1:p.Lys26380=
XM_024453094.1:c.100635A>G (TTN)	XP_024308862.1:p.Lys33545=
XM_024453095.1:c.100632A>G (TTN)	XP_024308863.1:p.Lys33544=
XM_024453096.1:c.100065A>G (TTN)	XP_024308864.1:p.Lys33355=
XM_024453097.1:c.97407A>G (TTN)	XP_024308865.1:p.Lys32469=
XM_024453098.1:c.97326A>G (TTN)	XP_024308866.1:p.Lys32442=
XM_024453099.1:c.79089A>G (TTN)	XP_024308867.1:p.Lys26363=
XM_024453100.1:c.68943A>G (TTN)	XP_024308868.1:p.Lys22981=