Canonical Allele Identifier: CA1310514525

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530339A= , CM000664.2:g.178530339A=	GRCh38
NC_000002.11:g.179395066A= , CM000664.1:g.179395066A=	GRCh37
NC_000002.10:g.179103312A=	NCBI36
NG_011618.3:g.305464T= , LRG_391:g.305464T=
NG_051363.1:g.12513A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98572T= (TTN)	ENSP00000343764.6:p.Leu32858=
ENST00000342175.11:c.79657T= (TTN)	ENSP00000340554.6:p.Leu26553=
ENST00000359218.10:c.79456T= (TTN)	ENSP00000352154.5:p.Leu26486=
ENST00000342175.10:c.79657T= (TTN)	ENSP00000340554.6:p.Leu26553=
ENST00000342992.10:c.98572T= (TTN)	ENSP00000343764.6:p.Leu32858=
ENST00000359218.9:c.79456T= (TTN)	ENSP00000352154.5:p.Leu26486=
ENST00000460472.6:c.79081T= (TTN)	ENSP00000434586.1:p.Leu26361=
ENST00000589042.5:c.106276T= (TTN) MANE Select	ENSP00000467141.1:p.Leu35426=
ENST00000591111.5:c.101353T= (TTN)	ENSP00000465570.1:p.Leu33785=
ENST00000615779.4:c.101353T= (TTN)	ENSP00000483597.1:p.Leu33785=
NM_001256850.1:c.101353T= (TTN)	NP_001243779.1:p.Leu33785=
NM_001267550.2:c.106276T= (TTN) MANE Select	NP_001254479.2:p.Leu35426=
NM_003319.4:c.79081T= (TTN)	NP_003310.4:p.Leu26361=
NM_133378.4:c.98572T= (TTN)	NP_596869.4:p.Leu32858=
NM_133432.3:c.79456T= (TTN)	NP_597676.3:p.Leu26486=
NM_133437.4:c.79657T= (TTN)	NP_597681.4:p.Leu26553=
NR_038271.1:n.446+6703A= (TTN-AS1)
NR_038272.1:n.220-5393A= (TTN-AS1)
XM_011511729.1:c.105373T= (TTN)	XP_011510031.1:p.Leu35125=
XM_011511730.1:c.79267T= (TTN)	XP_011510032.1:p.Leu26423=
XM_011511731.1:c.79126T= (TTN)	XP_011510033.1:p.Leu26376=
XM_017004819.1:c.105169T= (TTN)	XP_016860308.1:p.Leu35057=
XM_017004820.1:c.100567T= (TTN)	XP_016860309.1:p.Leu33523=
XM_017004821.1:c.100564T= (TTN)	XP_016860310.1:p.Leu33522=
XM_017004822.1:c.97606T= (TTN)	XP_016860311.1:p.Leu32536=
XM_017004823.1:c.79222T= (TTN)	XP_016860312.1:p.Leu26408=
XM_024453094.1:c.100717T= (TTN)	XP_024308862.1:p.Leu33573=
XM_024453095.1:c.100714T= (TTN)	XP_024308863.1:p.Leu33572=
XM_024453096.1:c.100147T= (TTN)	XP_024308864.1:p.Leu33383=
XM_024453097.1:c.97489T= (TTN)	XP_024308865.1:p.Leu32497=
XM_024453098.1:c.97408T= (TTN)	XP_024308866.1:p.Leu32470=
XM_024453099.1:c.79171T= (TTN)	XP_024308867.1:p.Leu26391=
XM_024453100.1:c.69025T= (TTN)	XP_024308868.1:p.Leu23009=