Canonical Allele Identifier: CA349406798

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395170T>C (hg19) ; chr2:g.178530443T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530443T>C , CM000664.2:g.178530443T>C	GRCh38
NC_000002.11:g.179395170T>C , CM000664.1:g.179395170T>C	GRCh37
NC_000002.10:g.179103416T>C	NCBI36
NG_011618.3:g.305360A>G , LRG_391:g.305360A>G
NG_051363.1:g.12617T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98468A>G (TTN)	ENSP00000343764.6:p.Glu32823Gly
ENST00000342175.11:c.79553A>G (TTN)	ENSP00000340554.6:p.Glu26518Gly
ENST00000359218.10:c.79352A>G (TTN)	ENSP00000352154.5:p.Glu26451Gly
ENST00000342175.10:c.79553A>G (TTN)	ENSP00000340554.6:p.Glu26518Gly
ENST00000342992.10:c.98468A>G (TTN)	ENSP00000343764.6:p.Glu32823Gly
ENST00000359218.9:c.79352A>G (TTN)	ENSP00000352154.5:p.Glu26451Gly
ENST00000460472.6:c.78977A>G (TTN)	ENSP00000434586.1:p.Glu26326Gly
ENST00000589042.5:c.106172A>G (TTN) MANE Select	ENSP00000467141.1:p.Glu35391Gly
ENST00000591111.5:c.101249A>G (TTN)	ENSP00000465570.1:p.Glu33750Gly
ENST00000615779.4:c.101249A>G (TTN)	ENSP00000483597.1:p.Glu33750Gly
NM_001256850.1:c.101249A>G (TTN)	NP_001243779.1:p.Glu33750Gly
NM_001267550.2:c.106172A>G (TTN) MANE Select	NP_001254479.2:p.Glu35391Gly
NM_003319.4:c.78977A>G (TTN)	NP_003310.4:p.Glu26326Gly
NM_133378.4:c.98468A>G (TTN)	NP_596869.4:p.Glu32823Gly
NM_133432.3:c.79352A>G (TTN)	NP_597676.3:p.Glu26451Gly
NM_133437.4:c.79553A>G (TTN)	NP_597681.4:p.Glu26518Gly
NR_038271.1:n.446+6807T>C (TTN-AS1)
NR_038272.1:n.220-5289T>C (TTN-AS1)
XM_011511729.1:c.105269A>G (TTN)	XP_011510031.1:p.Glu35090Gly
XM_011511730.1:c.79163A>G (TTN)	XP_011510032.1:p.Glu26388Gly
XM_011511731.1:c.79022A>G (TTN)	XP_011510033.1:p.Glu26341Gly
XM_017004819.1:c.105065A>G (TTN)	XP_016860308.1:p.Glu35022Gly
XM_017004820.1:c.100463A>G (TTN)	XP_016860309.1:p.Glu33488Gly
XM_017004821.1:c.100460A>G (TTN)	XP_016860310.1:p.Glu33487Gly
XM_017004822.1:c.97502A>G (TTN)	XP_016860311.1:p.Glu32501Gly
XM_017004823.1:c.79118A>G (TTN)	XP_016860312.1:p.Glu26373Gly
XM_024453094.1:c.100613A>G (TTN)	XP_024308862.1:p.Glu33538Gly
XM_024453095.1:c.100610A>G (TTN)	XP_024308863.1:p.Glu33537Gly
XM_024453096.1:c.100043A>G (TTN)	XP_024308864.1:p.Glu33348Gly
XM_024453097.1:c.97385A>G (TTN)	XP_024308865.1:p.Glu32462Gly
XM_024453098.1:c.97304A>G (TTN)	XP_024308866.1:p.Glu32435Gly
XM_024453099.1:c.79067A>G (TTN)	XP_024308867.1:p.Glu26356Gly
XM_024453100.1:c.68921A>G (TTN)	XP_024308868.1:p.Glu22974Gly