Canonical Allele Identifier: CA349481137

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179455833A>C (hg19) ; chr2:g.178591106A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591106A>C , CM000664.2:g.178591106A>C	GRCh38
NC_000002.11:g.179455833A>C , CM000664.1:g.179455833A>C	GRCh37
NC_000002.10:g.179164079A>C	NCBI36
NG_011618.3:g.244697T>G , LRG_391:g.244697T>G
NG_051363.1:g.73280A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52915T>G (TTN)	ENSP00000343764.6:p.Tyr17639Asp
ENST00000342175.11:c.34000T>G (TTN)	ENSP00000340554.6:p.Tyr11334Asp
ENST00000359218.10:c.33799T>G (TTN)	ENSP00000352154.5:p.Tyr11267Asp
ENST00000342175.10:c.34000T>G (TTN)	ENSP00000340554.6:p.Tyr11334Asp
ENST00000342992.10:c.52915T>G (TTN)	ENSP00000343764.6:p.Tyr17639Asp
ENST00000359218.9:c.33799T>G (TTN)	ENSP00000352154.5:p.Tyr11267Asp
ENST00000460472.6:c.33424T>G (TTN)	ENSP00000434586.1:p.Tyr11142Asp
ENST00000589042.5:c.60619T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr20207Asp
ENST00000591111.5:c.55696T>G (TTN)	ENSP00000465570.1:p.Tyr18566Asp
ENST00000615779.4:c.55696T>G (TTN)	ENSP00000483597.1:p.Tyr18566Asp
NM_001256850.1:c.55696T>G (TTN)	NP_001243779.1:p.Tyr18566Asp
NM_001267550.2:c.60619T>G (TTN) MANE Select	NP_001254479.2:p.Tyr20207Asp
NM_003319.4:c.33424T>G (TTN)	NP_003310.4:p.Tyr11142Asp
NM_133378.4:c.52915T>G (TTN)	NP_596869.4:p.Tyr17639Asp
NM_133432.3:c.33799T>G (TTN)	NP_597676.3:p.Tyr11267Asp
NM_133437.4:c.34000T>G (TTN)	NP_597681.4:p.Tyr11334Asp
NR_038271.1:n.597-6490A>C (TTN-AS1)
NR_038272.1:n.3189-33A>C (TTN-AS1)
XM_011511729.1:c.59716T>G (TTN)	XP_011510031.1:p.Tyr19906Asp
XM_011511730.1:c.33610T>G (TTN)	XP_011510032.1:p.Tyr11204Asp
XM_011511731.1:c.33469T>G (TTN)	XP_011510033.1:p.Tyr11157Asp
XM_017004819.1:c.59512T>G (TTN)	XP_016860308.1:p.Tyr19838Asp
XM_017004820.1:c.54910T>G (TTN)	XP_016860309.1:p.Tyr18304Asp
XM_017004821.1:c.54907T>G (TTN)	XP_016860310.1:p.Tyr18303Asp
XM_017004822.1:c.51949T>G (TTN)	XP_016860311.1:p.Tyr17317Asp
XM_017004823.1:c.33565T>G (TTN)	XP_016860312.1:p.Tyr11189Asp
XM_024453094.1:c.55060T>G (TTN)	XP_024308862.1:p.Tyr18354Asp
XM_024453095.1:c.55057T>G (TTN)	XP_024308863.1:p.Tyr18353Asp
XM_024453096.1:c.54490T>G (TTN)	XP_024308864.1:p.Tyr18164Asp
XM_024453097.1:c.51832T>G (TTN)	XP_024308865.1:p.Tyr17278Asp
XM_024453098.1:c.51751T>G (TTN)	XP_024308866.1:p.Tyr17251Asp
XM_024453099.1:c.33514T>G (TTN)	XP_024308867.1:p.Tyr11172Asp
XM_024453100.1:c.23368T>G (TTN)	XP_024308868.1:p.Tyr7790Asp