Canonical Allele Identifier: CA1310514616

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530418_178530420delinsGGT , CM000664.2:g.178530418_178530420delinsGGT	GRCh38
NC_000002.11:g.179395145_179395147delinsGGT , CM000664.1:g.179395145_179395147delinsGGT	GRCh37
NC_000002.10:g.179103391_179103393delinsGGT	NCBI36
NG_011618.3:g.305383_305385delinsACC , LRG_391:g.305383_305385delinsACC
NG_051363.1:g.12592_12594delinsGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98491_98493delinsACC (TTN)	ENSP00000343764.6:p.Thr32831=
ENST00000342175.11:c.79576_79578delinsACC (TTN)	ENSP00000340554.6:p.Thr26526=
ENST00000359218.10:c.79375_79377delinsACC (TTN)	ENSP00000352154.5:p.Thr26459=
ENST00000342175.10:c.79576_79578delinsACC (TTN)	ENSP00000340554.6:p.Thr26526=
ENST00000342992.10:c.98491_98493delinsACC (TTN)	ENSP00000343764.6:p.Thr32831=
ENST00000359218.9:c.79375_79377delinsACC (TTN)	ENSP00000352154.5:p.Thr26459=
ENST00000460472.6:c.79000_79002delinsACC (TTN)	ENSP00000434586.1:p.Thr26334=
ENST00000589042.5:c.106195_106197delinsACC (TTN) MANE Select	ENSP00000467141.1:p.Thr35399=
ENST00000591111.5:c.101272_101274delinsACC (TTN)	ENSP00000465570.1:p.Thr33758=
ENST00000615779.4:c.101272_101274delinsACC (TTN)	ENSP00000483597.1:p.Thr33758=
NM_001256850.1:c.101272_101274delinsACC (TTN)	NP_001243779.1:p.Thr33758=
NM_001267550.2:c.106195_106197delinsACC (TTN) MANE Select	NP_001254479.2:p.Thr35399=
NM_003319.4:c.79000_79002delinsACC (TTN)	NP_003310.4:p.Thr26334=
NM_133378.4:c.98491_98493delinsACC (TTN)	NP_596869.4:p.Thr32831=
NM_133432.3:c.79375_79377delinsACC (TTN)	NP_597676.3:p.Thr26459=
NM_133437.4:c.79576_79578delinsACC (TTN)	NP_597681.4:p.Thr26526=
NR_038271.1:n.446+6782_446+6784delinsGGT (TTN-AS1)
NR_038272.1:n.220-5314_220-5312delinsGGT (TTN-AS1)
XM_011511729.1:c.105292_105294delinsACC (TTN)	XP_011510031.1:p.Thr35098=
XM_011511730.1:c.79186_79188delinsACC (TTN)	XP_011510032.1:p.Thr26396=
XM_011511731.1:c.79045_79047delinsACC (TTN)	XP_011510033.1:p.Thr26349=
XM_017004819.1:c.105088_105090delinsACC (TTN)	XP_016860308.1:p.Thr35030=
XM_017004820.1:c.100486_100488delinsACC (TTN)	XP_016860309.1:p.Thr33496=
XM_017004821.1:c.100483_100485delinsACC (TTN)	XP_016860310.1:p.Thr33495=
XM_017004822.1:c.97525_97527delinsACC (TTN)	XP_016860311.1:p.Thr32509=
XM_017004823.1:c.79141_79143delinsACC (TTN)	XP_016860312.1:p.Thr26381=
XM_024453094.1:c.100636_100638delinsACC (TTN)	XP_024308862.1:p.Thr33546=
XM_024453095.1:c.100633_100635delinsACC (TTN)	XP_024308863.1:p.Thr33545=
XM_024453096.1:c.100066_100068delinsACC (TTN)	XP_024308864.1:p.Thr33356=
XM_024453097.1:c.97408_97410delinsACC (TTN)	XP_024308865.1:p.Thr32470=
XM_024453098.1:c.97327_97329delinsACC (TTN)	XP_024308866.1:p.Thr32443=
XM_024453099.1:c.79090_79092delinsACC (TTN)	XP_024308867.1:p.Thr26364=
XM_024453100.1:c.68944_68946delinsACC (TTN)	XP_024308868.1:p.Thr22982=