Canonical Allele Identifier: CA349410910

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396548T>G (hg19) ; chr2:g.178531821T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178531821T>G , CM000664.2:g.178531821T>G	GRCh38
NC_000002.11:g.179396548T>G , CM000664.1:g.179396548T>G	GRCh37
NC_000002.10:g.179104794T>G	NCBI36
NG_011618.3:g.303982A>C , LRG_391:g.303982A>C
NG_051363.1:g.13995T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.97090A>C (TTN)	ENSP00000343764.6:p.Ser32364Arg
ENST00000342175.11:c.78175A>C (TTN)	ENSP00000340554.6:p.Ser26059Arg
ENST00000359218.10:c.77974A>C (TTN)	ENSP00000352154.5:p.Ser25992Arg
ENST00000342175.10:c.78175A>C (TTN)	ENSP00000340554.6:p.Ser26059Arg
ENST00000342992.10:c.97090A>C (TTN)	ENSP00000343764.6:p.Ser32364Arg
ENST00000359218.9:c.77974A>C (TTN)	ENSP00000352154.5:p.Ser25992Arg
ENST00000460472.6:c.77599A>C (TTN)	ENSP00000434586.1:p.Ser25867Arg
ENST00000589042.5:c.104794A>C (TTN) MANE Select	ENSP00000467141.1:p.Ser34932Arg
ENST00000591111.5:c.99871A>C (TTN)	ENSP00000465570.1:p.Ser33291Arg
ENST00000615779.4:c.99871A>C (TTN)	ENSP00000483597.1:p.Ser33291Arg
NM_001256850.1:c.99871A>C (TTN)	NP_001243779.1:p.Ser33291Arg
NM_001267550.2:c.104794A>C (TTN) MANE Select	NP_001254479.2:p.Ser34932Arg
NM_003319.4:c.77599A>C (TTN)	NP_003310.4:p.Ser25867Arg
NM_133378.4:c.97090A>C (TTN)	NP_596869.4:p.Ser32364Arg
NM_133432.3:c.77974A>C (TTN)	NP_597676.3:p.Ser25992Arg
NM_133437.4:c.78175A>C (TTN)	NP_597681.4:p.Ser26059Arg
NR_038271.1:n.446+8185T>G (TTN-AS1)
NR_038272.1:n.220-3911T>G (TTN-AS1)
XM_011511729.1:c.103891A>C (TTN)	XP_011510031.1:p.Ser34631Arg
XM_011511730.1:c.77785A>C (TTN)	XP_011510032.1:p.Ser25929Arg
XM_011511731.1:c.77644A>C (TTN)	XP_011510033.1:p.Ser25882Arg
XM_017004819.1:c.103687A>C (TTN)	XP_016860308.1:p.Ser34563Arg
XM_017004820.1:c.99085A>C (TTN)	XP_016860309.1:p.Ser33029Arg
XM_017004821.1:c.99082A>C (TTN)	XP_016860310.1:p.Ser33028Arg
XM_017004822.1:c.96124A>C (TTN)	XP_016860311.1:p.Ser32042Arg
XM_017004823.1:c.77740A>C (TTN)	XP_016860312.1:p.Ser25914Arg
XM_024453094.1:c.99235A>C (TTN)	XP_024308862.1:p.Ser33079Arg
XM_024453095.1:c.99232A>C (TTN)	XP_024308863.1:p.Ser33078Arg
XM_024453096.1:c.98665A>C (TTN)	XP_024308864.1:p.Ser32889Arg
XM_024453097.1:c.96007A>C (TTN)	XP_024308865.1:p.Ser32003Arg
XM_024453098.1:c.95926A>C (TTN)	XP_024308866.1:p.Ser31976Arg
XM_024453099.1:c.77689A>C (TTN)	XP_024308867.1:p.Ser25897Arg
XM_024453100.1:c.67543A>C (TTN)	XP_024308868.1:p.Ser22515Arg