Canonical Allele Identifier: CA1986013

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178536118A>G , CM000664.2:g.178536118A>G	GRCh38
NC_000002.11:g.179400845A>G , CM000664.1:g.179400845A>G	GRCh37
NC_000002.10:g.179109091A>G	NCBI36
NG_011618.3:g.299685T>C , LRG_391:g.299685T>C
NG_051363.1:g.18292A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.100629T>C (TTN) MANE Select	NP_001254479.2:p.Tyr33543=
ENST00000589042.5:c.100629T>C (TTN) MANE Select	ENSP00000467141.1:p.Tyr33543=
NM_001256850.1:c.95706T>C (TTN)	NP_001243779.1:p.Tyr31902=
NM_003319.4:c.73434T>C (TTN)	NP_003310.4:p.Tyr24478=
NM_133378.4:c.92925T>C (TTN)	NP_596869.4:p.Tyr30975=
NM_133432.3:c.73809T>C (TTN)	NP_597676.3:p.Tyr24603=
NM_133437.4:c.74010T>C (TTN)	NP_597681.4:p.Tyr24670=
NR_038271.1:n.446+12482A>G (TTN-AS1)
NR_038272.1:n.316+290A>G (TTN-AS1)
ENST00000342175.10:c.74010T>C (TTN)	ENSP00000340554.6:p.Tyr24670=
ENST00000342175.11:c.74010T>C (TTN)	ENSP00000340554.6:p.Tyr24670=
ENST00000342992.10:c.92925T>C (TTN)	ENSP00000343764.6:p.Tyr30975=
ENST00000342992.11:c.92925T>C (TTN)	ENSP00000343764.6:p.Tyr30975=
ENST00000359218.10:c.73809T>C (TTN)	ENSP00000352154.5:p.Tyr24603=
ENST00000359218.9:c.73809T>C (TTN)	ENSP00000352154.5:p.Tyr24603=
ENST00000460472.6:c.73434T>C (TTN)	ENSP00000434586.1:p.Tyr24478=
ENST00000591111.5:c.95706T>C (TTN)	ENSP00000465570.1:p.Tyr31902=
ENST00000615779.4:c.95706T>C (TTN)	ENSP00000483597.1:p.Tyr31902=
XM_011511729.1:c.99726T>C (TTN)	XP_011510031.1:p.Tyr33242=
XM_011511730.1:c.73620T>C (TTN)	XP_011510032.1:p.Tyr24540=
XM_011511731.1:c.73479T>C (TTN)	XP_011510033.1:p.Tyr24493=
XM_017004819.1:c.99522T>C (TTN)	XP_016860308.1:p.Tyr33174=
XM_017004820.1:c.94920T>C (TTN)	XP_016860309.1:p.Tyr31640=
XM_017004821.1:c.94917T>C (TTN)	XP_016860310.1:p.Tyr31639=
XM_017004822.1:c.91959T>C (TTN)	XP_016860311.1:p.Tyr30653=
XM_017004823.1:c.73575T>C (TTN)	XP_016860312.1:p.Tyr24525=
XM_024453094.1:c.95070T>C (TTN)	XP_024308862.1:p.Tyr31690=
XM_024453095.1:c.95067T>C (TTN)	XP_024308863.1:p.Tyr31689=
XM_024453096.1:c.94500T>C (TTN)	XP_024308864.1:p.Tyr31500=
XM_024453097.1:c.91842T>C (TTN)	XP_024308865.1:p.Tyr30614=
XM_024453098.1:c.91761T>C (TTN)	XP_024308866.1:p.Tyr30587=
XM_024453099.1:c.73524T>C (TTN)	XP_024308867.1:p.Tyr24508=
XM_024453100.1:c.63378T>C (TTN)	XP_024308868.1:p.Tyr21126=