Canonical Allele Identifier: CA349411787

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396930C>G (hg19) ; chr2:g.178532203C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532203C>G , CM000664.2:g.178532203C>G	GRCh38
NC_000002.11:g.179396930C>G , CM000664.1:g.179396930C>G	GRCh37
NC_000002.10:g.179105176C>G	NCBI36
NG_011618.3:g.303600G>C , LRG_391:g.303600G>C
NG_051363.1:g.14377C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96708G>C (TTN)	ENSP00000343764.6:p.Arg32236Ser
ENST00000342175.11:c.77793G>C (TTN)	ENSP00000340554.6:p.Arg25931Ser
ENST00000359218.10:c.77592G>C (TTN)	ENSP00000352154.5:p.Arg25864Ser
ENST00000342175.10:c.77793G>C (TTN)	ENSP00000340554.6:p.Arg25931Ser
ENST00000342992.10:c.96708G>C (TTN)	ENSP00000343764.6:p.Arg32236Ser
ENST00000359218.9:c.77592G>C (TTN)	ENSP00000352154.5:p.Arg25864Ser
ENST00000460472.6:c.77217G>C (TTN)	ENSP00000434586.1:p.Arg25739Ser
ENST00000589042.5:c.104412G>C (TTN) MANE Select	ENSP00000467141.1:p.Arg34804Ser
ENST00000591111.5:c.99489G>C (TTN)	ENSP00000465570.1:p.Arg33163Ser
ENST00000615779.4:c.99489G>C (TTN)	ENSP00000483597.1:p.Arg33163Ser
NM_001256850.1:c.99489G>C (TTN)	NP_001243779.1:p.Arg33163Ser
NM_001267550.2:c.104412G>C (TTN) MANE Select	NP_001254479.2:p.Arg34804Ser
NM_003319.4:c.77217G>C (TTN)	NP_003310.4:p.Arg25739Ser
NM_133378.4:c.96708G>C (TTN)	NP_596869.4:p.Arg32236Ser
NM_133432.3:c.77592G>C (TTN)	NP_597676.3:p.Arg25864Ser
NM_133437.4:c.77793G>C (TTN)	NP_597681.4:p.Arg25931Ser
NR_038271.1:n.446+8567C>G (TTN-AS1)
NR_038272.1:n.220-3529C>G (TTN-AS1)
XM_011511729.1:c.103509G>C (TTN)	XP_011510031.1:p.Arg34503Ser
XM_011511730.1:c.77403G>C (TTN)	XP_011510032.1:p.Arg25801Ser
XM_011511731.1:c.77262G>C (TTN)	XP_011510033.1:p.Arg25754Ser
XM_017004819.1:c.103305G>C (TTN)	XP_016860308.1:p.Arg34435Ser
XM_017004820.1:c.98703G>C (TTN)	XP_016860309.1:p.Arg32901Ser
XM_017004821.1:c.98700G>C (TTN)	XP_016860310.1:p.Arg32900Ser
XM_017004822.1:c.95742G>C (TTN)	XP_016860311.1:p.Arg31914Ser
XM_017004823.1:c.77358G>C (TTN)	XP_016860312.1:p.Arg25786Ser
XM_024453094.1:c.98853G>C (TTN)	XP_024308862.1:p.Arg32951Ser
XM_024453095.1:c.98850G>C (TTN)	XP_024308863.1:p.Arg32950Ser
XM_024453096.1:c.98283G>C (TTN)	XP_024308864.1:p.Arg32761Ser
XM_024453097.1:c.95625G>C (TTN)	XP_024308865.1:p.Arg31875Ser
XM_024453098.1:c.95544G>C (TTN)	XP_024308866.1:p.Arg31848Ser
XM_024453099.1:c.77307G>C (TTN)	XP_024308867.1:p.Arg25769Ser
XM_024453100.1:c.67161G>C (TTN)	XP_024308868.1:p.Arg22387Ser