Canonical Allele Identifier: CA349407087

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395266C>G (hg19) ; chr2:g.178530539C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530539C>G , CM000664.2:g.178530539C>G	GRCh38
NC_000002.11:g.179395266C>G , CM000664.1:g.179395266C>G	GRCh37
NC_000002.10:g.179103512C>G	NCBI36
NG_011618.3:g.305264G>C , LRG_391:g.305264G>C
NG_051363.1:g.12713C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98372G>C (TTN)	ENSP00000343764.6:p.Cys32791Ser
ENST00000342175.11:c.79457G>C (TTN)	ENSP00000340554.6:p.Cys26486Ser
ENST00000359218.10:c.79256G>C (TTN)	ENSP00000352154.5:p.Cys26419Ser
ENST00000342175.10:c.79457G>C (TTN)	ENSP00000340554.6:p.Cys26486Ser
ENST00000342992.10:c.98372G>C (TTN)	ENSP00000343764.6:p.Cys32791Ser
ENST00000359218.9:c.79256G>C (TTN)	ENSP00000352154.5:p.Cys26419Ser
ENST00000460472.6:c.78881G>C (TTN)	ENSP00000434586.1:p.Cys26294Ser
ENST00000589042.5:c.106076G>C (TTN) MANE Select	ENSP00000467141.1:p.Cys35359Ser
ENST00000591111.5:c.101153G>C (TTN)	ENSP00000465570.1:p.Cys33718Ser
ENST00000615779.4:c.101153G>C (TTN)	ENSP00000483597.1:p.Cys33718Ser
NM_001256850.1:c.101153G>C (TTN)	NP_001243779.1:p.Cys33718Ser
NM_001267550.2:c.106076G>C (TTN) MANE Select	NP_001254479.2:p.Cys35359Ser
NM_003319.4:c.78881G>C (TTN)	NP_003310.4:p.Cys26294Ser
NM_133378.4:c.98372G>C (TTN)	NP_596869.4:p.Cys32791Ser
NM_133432.3:c.79256G>C (TTN)	NP_597676.3:p.Cys26419Ser
NM_133437.4:c.79457G>C (TTN)	NP_597681.4:p.Cys26486Ser
NR_038271.1:n.446+6903C>G (TTN-AS1)
NR_038272.1:n.220-5193C>G (TTN-AS1)
XM_011511729.1:c.105173G>C (TTN)	XP_011510031.1:p.Cys35058Ser
XM_011511730.1:c.79067G>C (TTN)	XP_011510032.1:p.Cys26356Ser
XM_011511731.1:c.78926G>C (TTN)	XP_011510033.1:p.Cys26309Ser
XM_017004819.1:c.104969G>C (TTN)	XP_016860308.1:p.Cys34990Ser
XM_017004820.1:c.100367G>C (TTN)	XP_016860309.1:p.Cys33456Ser
XM_017004821.1:c.100364G>C (TTN)	XP_016860310.1:p.Cys33455Ser
XM_017004822.1:c.97406G>C (TTN)	XP_016860311.1:p.Cys32469Ser
XM_017004823.1:c.79022G>C (TTN)	XP_016860312.1:p.Cys26341Ser
XM_024453094.1:c.100517G>C (TTN)	XP_024308862.1:p.Cys33506Ser
XM_024453095.1:c.100514G>C (TTN)	XP_024308863.1:p.Cys33505Ser
XM_024453096.1:c.99947G>C (TTN)	XP_024308864.1:p.Cys33316Ser
XM_024453097.1:c.97289G>C (TTN)	XP_024308865.1:p.Cys32430Ser
XM_024453098.1:c.97208G>C (TTN)	XP_024308866.1:p.Cys32403Ser
XM_024453099.1:c.78971G>C (TTN)	XP_024308867.1:p.Cys26324Ser
XM_024453100.1:c.68825G>C (TTN)	XP_024308868.1:p.Cys22942Ser