Canonical Allele Identifier: CA349524576

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178554522G>A , CM000664.2:g.178554522G>A	GRCh38
NC_000002.11:g.179419249G>A , CM000664.1:g.179419249G>A	GRCh37
NC_000002.10:g.179127495G>A	NCBI36
NG_011618.3:g.281281C>T , LRG_391:g.281281C>T
NG_051363.1:g.36696G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.88825C>T (TTN) MANE Select	NP_001254479.2:p.Arg29609Ter
ENST00000589042.5:c.88825C>T (TTN) MANE Select	ENSP00000467141.1:p.Arg29609Ter
NM_001256850.1:c.83902C>T (TTN)	NP_001243779.1:p.Arg27968Ter
NM_003319.4:c.61630C>T (TTN)	NP_003310.4:p.Arg20544Ter
NM_133378.4:c.81121C>T (TTN)	NP_596869.4:p.Arg27041Ter
NM_133432.3:c.62005C>T (TTN)	NP_597676.3:p.Arg20669Ter
NM_133437.4:c.62206C>T (TTN)	NP_597681.4:p.Arg20736Ter
NR_038271.1:n.447-16778G>A (TTN-AS1)
NR_038272.1:n.2043+12161G>A (TTN-AS1)
ENST00000342175.10:c.62206C>T (TTN)	ENSP00000340554.6:p.Arg20736Ter
ENST00000342175.11:c.62206C>T (TTN)	ENSP00000340554.6:p.Arg20736Ter
ENST00000342992.10:c.81121C>T (TTN)	ENSP00000343764.6:p.Arg27041Ter
ENST00000342992.11:c.81121C>T (TTN)	ENSP00000343764.6:p.Arg27041Ter
ENST00000359218.10:c.62005C>T (TTN)	ENSP00000352154.5:p.Arg20669Ter
ENST00000359218.9:c.62005C>T (TTN)	ENSP00000352154.5:p.Arg20669Ter
ENST00000460472.6:c.61630C>T (TTN)	ENSP00000434586.1:p.Arg20544Ter
ENST00000591111.5:c.83902C>T (TTN)	ENSP00000465570.1:p.Arg27968Ter
ENST00000615779.4:c.83902C>T (TTN)	ENSP00000483597.1:p.Arg27968Ter
XM_011511729.1:c.87922C>T (TTN)	XP_011510031.1:p.Arg29308Ter
XM_011511730.1:c.61816C>T (TTN)	XP_011510032.1:p.Arg20606Ter
XM_011511731.1:c.61675C>T (TTN)	XP_011510033.1:p.Arg20559Ter
XM_017004819.1:c.87718C>T (TTN)	XP_016860308.1:p.Arg29240Ter
XM_017004820.1:c.83116C>T (TTN)	XP_016860309.1:p.Arg27706Ter
XM_017004821.1:c.83113C>T (TTN)	XP_016860310.1:p.Arg27705Ter
XM_017004822.1:c.80155C>T (TTN)	XP_016860311.1:p.Arg26719Ter
XM_017004823.1:c.61771C>T (TTN)	XP_016860312.1:p.Arg20591Ter
XM_024453094.1:c.83266C>T (TTN)	XP_024308862.1:p.Arg27756Ter
XM_024453095.1:c.83263C>T (TTN)	XP_024308863.1:p.Arg27755Ter
XM_024453096.1:c.82696C>T (TTN)	XP_024308864.1:p.Arg27566Ter
XM_024453097.1:c.80038C>T (TTN)	XP_024308865.1:p.Arg26680Ter
XM_024453098.1:c.79957C>T (TTN)	XP_024308866.1:p.Arg26653Ter
XM_024453099.1:c.61720C>T (TTN)	XP_024308867.1:p.Arg20574Ter
XM_024453100.1:c.51574C>T (TTN)	XP_024308868.1:p.Arg17192Ter