Canonical Allele Identifier: CA089618

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178576614G>T , CM000664.2:g.178576614G>T	GRCh38
NC_000002.11:g.179441341G>T , CM000664.1:g.179441341G>T	GRCh37
NC_000002.10:g.179149587G>T	NCBI36
NG_011618.3:g.259189C>A , LRG_391:g.259189C>A
NG_051363.1:g.58788G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.61926C>A (TTN)	ENSP00000343764.6:p.Tyr20642Ter
ENST00000342175.11:c.43011C>A (TTN)	ENSP00000340554.6:p.Tyr14337Ter
ENST00000359218.10:c.42810C>A (TTN)	ENSP00000352154.5:p.Tyr14270Ter
ENST00000342175.10:c.43011C>A (TTN)	ENSP00000340554.6:p.Tyr14337Ter
ENST00000342992.10:c.61926C>A (TTN)	ENSP00000343764.6:p.Tyr20642Ter
ENST00000359218.9:c.42810C>A (TTN)	ENSP00000352154.5:p.Tyr14270Ter
ENST00000460472.6:c.42435C>A (TTN)	ENSP00000434586.1:p.Tyr14145Ter
ENST00000589042.5:c.69630C>A (TTN) MANE Select	ENSP00000467141.1:p.Tyr23210Ter
ENST00000591111.5:c.64707C>A (TTN)	ENSP00000465570.1:p.Tyr21569Ter
ENST00000615779.4:c.64707C>A (TTN)	ENSP00000483597.1:p.Tyr21569Ter
NM_001256850.1:c.64707C>A (TTN)	NP_001243779.1:p.Tyr21569Ter
NM_001267550.2:c.69630C>A (TTN) MANE Select	NP_001254479.2:p.Tyr23210Ter
NM_003319.4:c.42435C>A (TTN)	NP_003310.4:p.Tyr14145Ter
NM_133378.4:c.61926C>A (TTN)	NP_596869.4:p.Tyr20642Ter
NM_133432.3:c.42810C>A (TTN)	NP_597676.3:p.Tyr14270Ter
NM_133437.4:c.43011C>A (TTN)	NP_597681.4:p.Tyr14337Ter
NR_038271.1:n.596+5165G>T (TTN-AS1)
NR_038272.1:n.2044-5958G>T (TTN-AS1)
XM_011511729.1:c.68727C>A (TTN)	XP_011510031.1:p.Tyr22909Ter
XM_011511730.1:c.42621C>A (TTN)	XP_011510032.1:p.Tyr14207Ter
XM_011511731.1:c.42480C>A (TTN)	XP_011510033.1:p.Tyr14160Ter
XM_017004819.1:c.68523C>A (TTN)	XP_016860308.1:p.Tyr22841Ter
XM_017004820.1:c.63921C>A (TTN)	XP_016860309.1:p.Tyr21307Ter
XM_017004821.1:c.63918C>A (TTN)	XP_016860310.1:p.Tyr21306Ter
XM_017004822.1:c.60960C>A (TTN)	XP_016860311.1:p.Tyr20320Ter
XM_017004823.1:c.42576C>A (TTN)	XP_016860312.1:p.Tyr14192Ter
XM_024453094.1:c.64071C>A (TTN)	XP_024308862.1:p.Tyr21357Ter
XM_024453095.1:c.64068C>A (TTN)	XP_024308863.1:p.Tyr21356Ter
XM_024453096.1:c.63501C>A (TTN)	XP_024308864.1:p.Tyr21167Ter
XM_024453097.1:c.60843C>A (TTN)	XP_024308865.1:p.Tyr20281Ter
XM_024453098.1:c.60762C>A (TTN)	XP_024308866.1:p.Tyr20254Ter
XM_024453099.1:c.42525C>A (TTN)	XP_024308867.1:p.Tyr14175Ter
XM_024453100.1:c.32379C>A (TTN)	XP_024308868.1:p.Tyr10793Ter