Canonical Allele Identifier: CA349658782

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179439631A>G (hg19) ; chr2:g.178574904A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178574904A>G , CM000664.2:g.178574904A>G	GRCh38
NC_000002.11:g.179439631A>G , CM000664.1:g.179439631A>G	GRCh37
NC_000002.10:g.179147877A>G	NCBI36
NG_011618.3:g.260899T>C , LRG_391:g.260899T>C
NG_051363.1:g.57078A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.63524T>C (TTN)	ENSP00000343764.6:p.Phe21175Ser
ENST00000342175.11:c.44609T>C (TTN)	ENSP00000340554.6:p.Phe14870Ser
ENST00000359218.10:c.44408T>C (TTN)	ENSP00000352154.5:p.Phe14803Ser
ENST00000342175.10:c.44609T>C (TTN)	ENSP00000340554.6:p.Phe14870Ser
ENST00000342992.10:c.63524T>C (TTN)	ENSP00000343764.6:p.Phe21175Ser
ENST00000359218.9:c.44408T>C (TTN)	ENSP00000352154.5:p.Phe14803Ser
ENST00000460472.6:c.44033T>C (TTN)	ENSP00000434586.1:p.Phe14678Ser
ENST00000589042.5:c.71228T>C (TTN) MANE Select	ENSP00000467141.1:p.Phe23743Ser
ENST00000591111.5:c.66305T>C (TTN)	ENSP00000465570.1:p.Phe22102Ser
ENST00000615779.4:c.66305T>C (TTN)	ENSP00000483597.1:p.Phe22102Ser
NM_001256850.1:c.66305T>C (TTN)	NP_001243779.1:p.Phe22102Ser
NM_001267550.2:c.71228T>C (TTN) MANE Select	NP_001254479.2:p.Phe23743Ser
NM_003319.4:c.44033T>C (TTN)	NP_003310.4:p.Phe14678Ser
NM_133378.4:c.63524T>C (TTN)	NP_596869.4:p.Phe21175Ser
NM_133432.3:c.44408T>C (TTN)	NP_597676.3:p.Phe14803Ser
NM_133437.4:c.44609T>C (TTN)	NP_597681.4:p.Phe14870Ser
NR_038271.1:n.596+3455A>G (TTN-AS1)
NR_038272.1:n.2044-7668A>G (TTN-AS1)
XM_011511729.1:c.70325T>C (TTN)	XP_011510031.1:p.Phe23442Ser
XM_011511730.1:c.44219T>C (TTN)	XP_011510032.1:p.Phe14740Ser
XM_011511731.1:c.44078T>C (TTN)	XP_011510033.1:p.Phe14693Ser
XM_017004819.1:c.70121T>C (TTN)	XP_016860308.1:p.Phe23374Ser
XM_017004820.1:c.65519T>C (TTN)	XP_016860309.1:p.Phe21840Ser
XM_017004821.1:c.65516T>C (TTN)	XP_016860310.1:p.Phe21839Ser
XM_017004822.1:c.62558T>C (TTN)	XP_016860311.1:p.Phe20853Ser
XM_017004823.1:c.44174T>C (TTN)	XP_016860312.1:p.Phe14725Ser
XM_024453094.1:c.65669T>C (TTN)	XP_024308862.1:p.Phe21890Ser
XM_024453095.1:c.65666T>C (TTN)	XP_024308863.1:p.Phe21889Ser
XM_024453096.1:c.65099T>C (TTN)	XP_024308864.1:p.Phe21700Ser
XM_024453097.1:c.62441T>C (TTN)	XP_024308865.1:p.Phe20814Ser
XM_024453098.1:c.62360T>C (TTN)	XP_024308866.1:p.Phe20787Ser
XM_024453099.1:c.44123T>C (TTN)	XP_024308867.1:p.Phe14708Ser
XM_024453100.1:c.33977T>C (TTN)	XP_024308868.1:p.Phe11326Ser