Canonical Allele Identifier: CA1310514732

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530546A= , CM000664.2:g.178530546A=	GRCh38
NC_000002.11:g.179395273A= , CM000664.1:g.179395273A=	GRCh37
NC_000002.10:g.179103519A=	NCBI36
NG_011618.3:g.305257T= , LRG_391:g.305257T=
NG_051363.1:g.12720A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98365T= (TTN)	ENSP00000343764.6:p.Tyr32789=
ENST00000342175.11:c.79450T= (TTN)	ENSP00000340554.6:p.Tyr26484=
ENST00000359218.10:c.79249T= (TTN)	ENSP00000352154.5:p.Tyr26417=
ENST00000342175.10:c.79450T= (TTN)	ENSP00000340554.6:p.Tyr26484=
ENST00000342992.10:c.98365T= (TTN)	ENSP00000343764.6:p.Tyr32789=
ENST00000359218.9:c.79249T= (TTN)	ENSP00000352154.5:p.Tyr26417=
ENST00000460472.6:c.78874T= (TTN)	ENSP00000434586.1:p.Tyr26292=
ENST00000589042.5:c.106069T= (TTN) MANE Select	ENSP00000467141.1:p.Tyr35357=
ENST00000591111.5:c.101146T= (TTN)	ENSP00000465570.1:p.Tyr33716=
ENST00000615779.4:c.101146T= (TTN)	ENSP00000483597.1:p.Tyr33716=
NM_001256850.1:c.101146T= (TTN)	NP_001243779.1:p.Tyr33716=
NM_001267550.2:c.106069T= (TTN) MANE Select	NP_001254479.2:p.Tyr35357=
NM_003319.4:c.78874T= (TTN)	NP_003310.4:p.Tyr26292=
NM_133378.4:c.98365T= (TTN)	NP_596869.4:p.Tyr32789=
NM_133432.3:c.79249T= (TTN)	NP_597676.3:p.Tyr26417=
NM_133437.4:c.79450T= (TTN)	NP_597681.4:p.Tyr26484=
NR_038271.1:n.446+6910A= (TTN-AS1)
NR_038272.1:n.220-5186A= (TTN-AS1)
XM_011511729.1:c.105166T= (TTN)	XP_011510031.1:p.Tyr35056=
XM_011511730.1:c.79060T= (TTN)	XP_011510032.1:p.Tyr26354=
XM_011511731.1:c.78919T= (TTN)	XP_011510033.1:p.Tyr26307=
XM_017004819.1:c.104962T= (TTN)	XP_016860308.1:p.Tyr34988=
XM_017004820.1:c.100360T= (TTN)	XP_016860309.1:p.Tyr33454=
XM_017004821.1:c.100357T= (TTN)	XP_016860310.1:p.Tyr33453=
XM_017004822.1:c.97399T= (TTN)	XP_016860311.1:p.Tyr32467=
XM_017004823.1:c.79015T= (TTN)	XP_016860312.1:p.Tyr26339=
XM_024453094.1:c.100510T= (TTN)	XP_024308862.1:p.Tyr33504=
XM_024453095.1:c.100507T= (TTN)	XP_024308863.1:p.Tyr33503=
XM_024453096.1:c.99940T= (TTN)	XP_024308864.1:p.Tyr33314=
XM_024453097.1:c.97282T= (TTN)	XP_024308865.1:p.Tyr32428=
XM_024453098.1:c.97201T= (TTN)	XP_024308866.1:p.Tyr32401=
XM_024453099.1:c.78964T= (TTN)	XP_024308867.1:p.Tyr26322=
XM_024453100.1:c.68818T= (TTN)	XP_024308868.1:p.Tyr22940=