Canonical Allele Identifier: CA1310521529

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544347G= , CM000664.2:g.178544347G=	GRCh38
NC_000002.11:g.179409074G= , CM000664.1:g.179409074G=	GRCh37
NC_000002.10:g.179117320G=	NCBI36
NG_011618.3:g.291456C= , LRG_391:g.291456C=
NG_051363.1:g.26521G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88178C= (TTN)	ENSP00000343764.6:p.Thr29393=
ENST00000342175.11:c.69263C= (TTN)	ENSP00000340554.6:p.Thr23088=
ENST00000359218.10:c.69062C= (TTN)	ENSP00000352154.5:p.Thr23021=
ENST00000342175.10:c.69263C= (TTN)	ENSP00000340554.6:p.Thr23088=
ENST00000342992.10:c.88178C= (TTN)	ENSP00000343764.6:p.Thr29393=
ENST00000359218.9:c.69062C= (TTN)	ENSP00000352154.5:p.Thr23021=
ENST00000460472.6:c.68687C= (TTN)	ENSP00000434586.1:p.Thr22896=
ENST00000589042.5:c.95882C= (TTN) MANE Select	ENSP00000467141.1:p.Thr31961=
ENST00000591111.5:c.90959C= (TTN)	ENSP00000465570.1:p.Thr30320=
ENST00000615779.4:c.90959C= (TTN)	ENSP00000483597.1:p.Thr30320=
NM_001256850.1:c.90959C= (TTN)	NP_001243779.1:p.Thr30320=
NM_001267550.2:c.95882C= (TTN) MANE Select	NP_001254479.2:p.Thr31961=
NM_003319.4:c.68687C= (TTN)	NP_003310.4:p.Thr22896=
NM_133378.4:c.88178C= (TTN)	NP_596869.4:p.Thr29393=
NM_133432.3:c.69062C= (TTN)	NP_597676.3:p.Thr23021=
NM_133437.4:c.69263C= (TTN)	NP_597681.4:p.Thr23088=
NR_038271.1:n.446+20711G= (TTN-AS1)
NR_038272.1:n.2043+1986G= (TTN-AS1)
XM_011511729.1:c.94979C= (TTN)	XP_011510031.1:p.Thr31660=
XM_011511730.1:c.68873C= (TTN)	XP_011510032.1:p.Thr22958=
XM_011511731.1:c.68732C= (TTN)	XP_011510033.1:p.Thr22911=
XM_017004819.1:c.94775C= (TTN)	XP_016860308.1:p.Thr31592=
XM_017004820.1:c.90173C= (TTN)	XP_016860309.1:p.Thr30058=
XM_017004821.1:c.90170C= (TTN)	XP_016860310.1:p.Thr30057=
XM_017004822.1:c.87212C= (TTN)	XP_016860311.1:p.Thr29071=
XM_017004823.1:c.68828C= (TTN)	XP_016860312.1:p.Thr22943=
XM_024453094.1:c.90323C= (TTN)	XP_024308862.1:p.Thr30108=
XM_024453095.1:c.90320C= (TTN)	XP_024308863.1:p.Thr30107=
XM_024453096.1:c.89753C= (TTN)	XP_024308864.1:p.Thr29918=
XM_024453097.1:c.87095C= (TTN)	XP_024308865.1:p.Thr29032=
XM_024453098.1:c.87014C= (TTN)	XP_024308866.1:p.Thr29005=
XM_024453099.1:c.68777C= (TTN)	XP_024308867.1:p.Thr22926=
XM_024453100.1:c.58631C= (TTN)	XP_024308868.1:p.Thr19544=