Canonical Allele Identifier: CA349454945

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408944C>G (hg19) ; chr2:g.178544217C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544217C>G , CM000664.2:g.178544217C>G	GRCh38
NC_000002.11:g.179408944C>G , CM000664.1:g.179408944C>G	GRCh37
NC_000002.10:g.179117190C>G	NCBI36
NG_011618.3:g.291586G>C , LRG_391:g.291586G>C
NG_051363.1:g.26391C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88308G>C (TTN)	ENSP00000343764.6:p.Glu29436Asp
ENST00000342175.11:c.69393G>C (TTN)	ENSP00000340554.6:p.Glu23131Asp
ENST00000359218.10:c.69192G>C (TTN)	ENSP00000352154.5:p.Glu23064Asp
ENST00000342175.10:c.69393G>C (TTN)	ENSP00000340554.6:p.Glu23131Asp
ENST00000342992.10:c.88308G>C (TTN)	ENSP00000343764.6:p.Glu29436Asp
ENST00000359218.9:c.69192G>C (TTN)	ENSP00000352154.5:p.Glu23064Asp
ENST00000460472.6:c.68817G>C (TTN)	ENSP00000434586.1:p.Glu22939Asp
ENST00000589042.5:c.96012G>C (TTN) MANE Select	ENSP00000467141.1:p.Glu32004Asp
ENST00000591111.5:c.91089G>C (TTN)	ENSP00000465570.1:p.Glu30363Asp
ENST00000615779.4:c.91089G>C (TTN)	ENSP00000483597.1:p.Glu30363Asp
NM_001256850.1:c.91089G>C (TTN)	NP_001243779.1:p.Glu30363Asp
NM_001267550.2:c.96012G>C (TTN) MANE Select	NP_001254479.2:p.Glu32004Asp
NM_003319.4:c.68817G>C (TTN)	NP_003310.4:p.Glu22939Asp
NM_133378.4:c.88308G>C (TTN)	NP_596869.4:p.Glu29436Asp
NM_133432.3:c.69192G>C (TTN)	NP_597676.3:p.Glu23064Asp
NM_133437.4:c.69393G>C (TTN)	NP_597681.4:p.Glu23131Asp
NR_038271.1:n.446+20581C>G (TTN-AS1)
NR_038272.1:n.2043+1856C>G (TTN-AS1)
XM_011511729.1:c.95109G>C (TTN)	XP_011510031.1:p.Glu31703Asp
XM_011511730.1:c.69003G>C (TTN)	XP_011510032.1:p.Glu23001Asp
XM_011511731.1:c.68862G>C (TTN)	XP_011510033.1:p.Glu22954Asp
XM_017004819.1:c.94905G>C (TTN)	XP_016860308.1:p.Glu31635Asp
XM_017004820.1:c.90303G>C (TTN)	XP_016860309.1:p.Glu30101Asp
XM_017004821.1:c.90300G>C (TTN)	XP_016860310.1:p.Glu30100Asp
XM_017004822.1:c.87342G>C (TTN)	XP_016860311.1:p.Glu29114Asp
XM_017004823.1:c.68958G>C (TTN)	XP_016860312.1:p.Glu22986Asp
XM_024453094.1:c.90453G>C (TTN)	XP_024308862.1:p.Glu30151Asp
XM_024453095.1:c.90450G>C (TTN)	XP_024308863.1:p.Glu30150Asp
XM_024453096.1:c.89883G>C (TTN)	XP_024308864.1:p.Glu29961Asp
XM_024453097.1:c.87225G>C (TTN)	XP_024308865.1:p.Glu29075Asp
XM_024453098.1:c.87144G>C (TTN)	XP_024308866.1:p.Glu29048Asp
XM_024453099.1:c.68907G>C (TTN)	XP_024308867.1:p.Glu22969Asp
XM_024453100.1:c.58761G>C (TTN)	XP_024308868.1:p.Glu19587Asp