Canonical Allele Identifier: CA1310550891

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618055T= , CM000664.2:g.178618055T=	GRCh38
NC_000002.11:g.179482782T= , CM000664.1:g.179482782T=	GRCh37
NC_000002.10:g.179191027T=	NCBI36
NG_011618.3:g.217748A= , LRG_391:g.217748A=
NG_051363.1:g.100229T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39592A= (TTN)	ENSP00000343764.6:p.Thr13198=
ENST00000342175.11:c.20677A= (TTN)	ENSP00000340554.6:p.Thr6893=
ENST00000359218.10:c.20476A= (TTN)	ENSP00000352154.5:p.Thr6826=
ENST00000342175.10:c.20677A= (TTN)	ENSP00000340554.6:p.Thr6893=
ENST00000342992.10:c.39592A= (TTN)	ENSP00000343764.6:p.Thr13198=
ENST00000359218.9:c.20476A= (TTN)	ENSP00000352154.5:p.Thr6826=
ENST00000460472.6:c.20101A= (TTN)	ENSP00000434586.1:p.Thr6701=
ENST00000589042.5:c.47296A= (TTN) MANE Select	ENSP00000467141.1:p.Thr15766=
ENST00000591111.5:c.42373A= (TTN)	ENSP00000465570.1:p.Thr14125=
ENST00000615779.4:c.42373A= (TTN)	ENSP00000483597.1:p.Thr14125=
NM_001256850.1:c.42373A= (TTN)	NP_001243779.1:p.Thr14125=
NM_001267550.2:c.47296A= (TTN) MANE Select	NP_001254479.2:p.Thr15766=
NM_003319.4:c.20101A= (TTN)	NP_003310.4:p.Thr6701=
NM_133378.4:c.39592A= (TTN)	NP_596869.4:p.Thr13198=
NM_133432.3:c.20476A= (TTN)	NP_597676.3:p.Thr6826=
NM_133437.4:c.20677A= (TTN)	NP_597681.4:p.Thr6893=
NR_038271.1:n.1605-1698T= (TTN-AS1)
XM_011511729.1:c.46393A= (TTN)	XP_011510031.1:p.Thr15465=
XM_011511730.1:c.20287A= (TTN)	XP_011510032.1:p.Thr6763=
XM_011511731.1:c.20146A= (TTN)	XP_011510033.1:p.Thr6716=
XM_017004819.1:c.46189A= (TTN)	XP_016860308.1:p.Thr15397=
XM_017004820.1:c.41587A= (TTN)	XP_016860309.1:p.Thr13863=
XM_017004821.1:c.41584A= (TTN)	XP_016860310.1:p.Thr13862=
XM_017004822.1:c.38626A= (TTN)	XP_016860311.1:p.Thr12876=
XM_017004823.1:c.20242A= (TTN)	XP_016860312.1:p.Thr6748=
XM_024453094.1:c.41737A= (TTN)	XP_024308862.1:p.Thr13913=
XM_024453095.1:c.41734A= (TTN)	XP_024308863.1:p.Thr13912=
XM_024453096.1:c.41167A= (TTN)	XP_024308864.1:p.Thr13723=
XM_024453097.1:c.38509A= (TTN)	XP_024308865.1:p.Thr12837=
XM_024453098.1:c.38428A= (TTN)	XP_024308866.1:p.Thr12810=
XM_024453099.1:c.20191A= (TTN)	XP_024308867.1:p.Thr6731=
XM_024453100.1:c.10045A= (TTN)	XP_024308868.1:p.Thr3349=