Canonical Allele Identifier: CA349574125

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178608604A>G , CM000664.2:g.178608604A>G	GRCh38
NC_000002.11:g.179473331A>G , CM000664.1:g.179473331A>G	GRCh37
NC_000002.10:g.179181576A>G	NCBI36
NG_011618.3:g.227199T>C , LRG_391:g.227199T>C
NG_051363.1:g.90778A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.52405+2T>C (TTN) MANE Select	NP_001254479.2:n.52405+2T>C
ENST00000589042.5:c.52405+2T>C (TTN) MANE Select	ENSP00000467141.1:n.52405+2T>C
NM_001256850.1:c.47482+2T>C (TTN)	NP_001243779.1:n.47482+2T>C
NM_003319.4:c.25210+2T>C (TTN)	NP_003310.4:n.25210+2T>C
NM_133378.4:c.44701+2T>C (TTN)	NP_596869.4:n.44701+2T>C
NM_133432.3:c.25585+2T>C (TTN)	NP_597676.3:n.25585+2T>C
NM_133437.4:c.25786+2T>C (TTN)	NP_597681.4:n.25786+2T>C
NR_038271.1:n.782+338A>G (TTN-AS1)
ENST00000342175.10:c.25786+2T>C (TTN)	ENSP00000340554.6:n.25786+2T>C
ENST00000342175.11:c.25786+2T>C (TTN)	ENSP00000340554.6:n.25786+2T>C
ENST00000342992.10:c.44701+2T>C (TTN)	ENSP00000343764.6:n.44701+2T>C
ENST00000342992.11:c.44701+2T>C (TTN)	ENSP00000343764.6:n.44701+2T>C
ENST00000359218.10:c.25585+2T>C (TTN)	ENSP00000352154.5:n.25585+2T>C
ENST00000359218.9:c.25585+2T>C (TTN)	ENSP00000352154.5:n.25585+2T>C
ENST00000460472.6:c.25210+2T>C (TTN)	ENSP00000434586.1:n.25210+2T>C
ENST00000591111.5:c.47482+2T>C (TTN)	ENSP00000465570.1:n.47482+2T>C
ENST00000615779.4:c.47482+2T>C (TTN)	ENSP00000483597.1:n.47482+2T>C
XM_011511729.1:c.51502+2T>C (TTN)	XP_011510031.1:n.51502+2T>C
XM_011511730.1:c.25396+2T>C (TTN)	XP_011510032.1:n.25396+2T>C
XM_011511731.1:c.25255+2T>C (TTN)	XP_011510033.1:n.25255+2T>C
XM_017004819.1:c.51298+2T>C (TTN)	XP_016860308.1:n.51298+2T>C
XM_017004820.1:c.46696+2T>C (TTN)	XP_016860309.1:n.46696+2T>C
XM_017004821.1:c.46693+2T>C (TTN)	XP_016860310.1:n.46693+2T>C
XM_017004822.1:c.43735+2T>C (TTN)	XP_016860311.1:n.43735+2T>C
XM_017004823.1:c.25351+2T>C (TTN)	XP_016860312.1:n.25351+2T>C
XM_024453094.1:c.46846+2T>C (TTN)	XP_024308862.1:n.46846+2T>C
XM_024453095.1:c.46843+2T>C (TTN)	XP_024308863.1:n.46843+2T>C
XM_024453096.1:c.46276+2T>C (TTN)	XP_024308864.1:n.46276+2T>C
XM_024453097.1:c.43618+2T>C (TTN)	XP_024308865.1:n.43618+2T>C
XM_024453098.1:c.43537+2T>C (TTN)	XP_024308866.1:n.43537+2T>C
XM_024453099.1:c.25300+2T>C (TTN)	XP_024308867.1:n.25300+2T>C
XM_024453100.1:c.15154+2T>C (TTN)	XP_024308868.1:n.15154+2T>C