Canonical Allele Identifier: CA349617180

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178617937C>T , CM000664.2:g.178617937C>T	GRCh38
NC_000002.11:g.179482664C>T , CM000664.1:g.179482664C>T	GRCh37
NC_000002.10:g.179190909C>T	NCBI36
NG_011618.3:g.217866G>A , LRG_391:g.217866G>A
NG_051363.1:g.100111C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.47414G>A (TTN) MANE Select	NP_001254479.2:p.Trp15805Ter
ENST00000589042.5:c.47414G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp15805Ter
NM_001256850.1:c.42491G>A (TTN)	NP_001243779.1:p.Trp14164Ter
NM_003319.4:c.20219G>A (TTN)	NP_003310.4:p.Trp6740Ter
NM_133378.4:c.39710G>A (TTN)	NP_596869.4:p.Trp13237Ter
NM_133432.3:c.20594G>A (TTN)	NP_597676.3:p.Trp6865Ter
NM_133437.4:c.20795G>A (TTN)	NP_597681.4:p.Trp6932Ter
NR_038271.1:n.1605-1816C>T (TTN-AS1)
ENST00000342175.10:c.20795G>A (TTN)	ENSP00000340554.6:p.Trp6932Ter
ENST00000342175.11:c.20795G>A (TTN)	ENSP00000340554.6:p.Trp6932Ter
ENST00000342992.10:c.39710G>A (TTN)	ENSP00000343764.6:p.Trp13237Ter
ENST00000342992.11:c.39710G>A (TTN)	ENSP00000343764.6:p.Trp13237Ter
ENST00000359218.10:c.20594G>A (TTN)	ENSP00000352154.5:p.Trp6865Ter
ENST00000359218.9:c.20594G>A (TTN)	ENSP00000352154.5:p.Trp6865Ter
ENST00000460472.6:c.20219G>A (TTN)	ENSP00000434586.1:p.Trp6740Ter
ENST00000591111.5:c.42491G>A (TTN)	ENSP00000465570.1:p.Trp14164Ter
ENST00000615779.4:c.42491G>A (TTN)	ENSP00000483597.1:p.Trp14164Ter
XM_011511729.1:c.46511G>A (TTN)	XP_011510031.1:p.Trp15504Ter
XM_011511730.1:c.20405G>A (TTN)	XP_011510032.1:p.Trp6802Ter
XM_011511731.1:c.20264G>A (TTN)	XP_011510033.1:p.Trp6755Ter
XM_017004819.1:c.46307G>A (TTN)	XP_016860308.1:p.Trp15436Ter
XM_017004820.1:c.41705G>A (TTN)	XP_016860309.1:p.Trp13902Ter
XM_017004821.1:c.41702G>A (TTN)	XP_016860310.1:p.Trp13901Ter
XM_017004822.1:c.38744G>A (TTN)	XP_016860311.1:p.Trp12915Ter
XM_017004823.1:c.20360G>A (TTN)	XP_016860312.1:p.Trp6787Ter
XM_024453094.1:c.41855G>A (TTN)	XP_024308862.1:p.Trp13952Ter
XM_024453095.1:c.41852G>A (TTN)	XP_024308863.1:p.Trp13951Ter
XM_024453096.1:c.41285G>A (TTN)	XP_024308864.1:p.Trp13762Ter
XM_024453097.1:c.38627G>A (TTN)	XP_024308865.1:p.Trp12876Ter
XM_024453098.1:c.38546G>A (TTN)	XP_024308866.1:p.Trp12849Ter
XM_024453099.1:c.20309G>A (TTN)	XP_024308867.1:p.Trp6770Ter
XM_024453100.1:c.10163G>A (TTN)	XP_024308868.1:p.Trp3388Ter