Canonical Allele Identifier: CA1310514304

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527107C= , CM000664.2:g.178527107C=	GRCh38
NC_000002.11:g.179391834C= , CM000664.1:g.179391834C=	GRCh37
NC_000002.10:g.179100080C=	NCBI36
NG_011618.3:g.308696G= , LRG_391:g.308696G=
NG_051363.1:g.9281C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.100177G= (TTN)	ENSP00000343764.6:p.Val33393=
ENST00000342175.11:c.81262G= (TTN)	ENSP00000340554.6:p.Val27088=
ENST00000359218.10:c.81061G= (TTN)	ENSP00000352154.5:p.Val27021=
ENST00000342175.10:c.81262G= (TTN)	ENSP00000340554.6:p.Val27088=
ENST00000342992.10:c.100177G= (TTN)	ENSP00000343764.6:p.Val33393=
ENST00000359218.9:c.81061G= (TTN)	ENSP00000352154.5:p.Val27021=
ENST00000460472.6:c.80686G= (TTN)	ENSP00000434586.1:p.Val26896=
ENST00000589042.5:c.107881G= (TTN) MANE Select	ENSP00000467141.1:p.Val35961=
ENST00000591111.5:c.102958G= (TTN)	ENSP00000465570.1:p.Val34320=
ENST00000615779.4:c.102958G= (TTN)	ENSP00000483597.1:p.Val34320=
NM_001256850.1:c.102958G= (TTN)	NP_001243779.1:p.Val34320=
NM_001267550.2:c.107881G= (TTN) MANE Select	NP_001254479.2:p.Val35961=
NM_003319.4:c.80686G= (TTN)	NP_003310.4:p.Val26896=
NM_133378.4:c.100177G= (TTN)	NP_596869.4:p.Val33393=
NM_133432.3:c.81061G= (TTN)	NP_597676.3:p.Val27021=
NM_133437.4:c.81262G= (TTN)	NP_597681.4:p.Val27088=
NR_038271.1:n.446+3471C= (TTN-AS1)
NR_038272.1:n.219+3471C= (TTN-AS1)
XM_011511729.1:c.106978G= (TTN)	XP_011510031.1:p.Val35660=
XM_011511730.1:c.80872G= (TTN)	XP_011510032.1:p.Val26958=
XM_011511731.1:c.80731G= (TTN)	XP_011510033.1:p.Val26911=
XM_017004819.1:c.106774G= (TTN)	XP_016860308.1:p.Val35592=
XM_017004820.1:c.102172G= (TTN)	XP_016860309.1:p.Val34058=
XM_017004821.1:c.102169G= (TTN)	XP_016860310.1:p.Val34057=
XM_017004822.1:c.99211G= (TTN)	XP_016860311.1:p.Val33071=
XM_017004823.1:c.80827G= (TTN)	XP_016860312.1:p.Val26943=
XM_024453094.1:c.102322G= (TTN)	XP_024308862.1:p.Val34108=
XM_024453095.1:c.102319G= (TTN)	XP_024308863.1:p.Val34107=
XM_024453096.1:c.101752G= (TTN)	XP_024308864.1:p.Val33918=
XM_024453097.1:c.99094G= (TTN)	XP_024308865.1:p.Val33032=
XM_024453098.1:c.99013G= (TTN)	XP_024308866.1:p.Val33005=
XM_024453099.1:c.80776G= (TTN)	XP_024308867.1:p.Val26926=
XM_024453100.1:c.70630G= (TTN)	XP_024308868.1:p.Val23544=