Canonical Allele Identifier: CA1310549454

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614650_178614651delinsAG , CM000664.2:g.178614650_178614651delinsAG	GRCh38
NC_000002.11:g.179479377_179479378delinsAG , CM000664.1:g.179479377_179479378delinsAG	GRCh37
NC_000002.10:g.179187622_179187623delinsAG	NCBI36
NG_011618.3:g.221152_221153delinsCT , LRG_391:g.221152_221153delinsCT
NG_051363.1:g.96824_96825delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.41159_41160delinsCT (TTN)	ENSP00000343764.6:p.Pro13720=
ENST00000342175.11:c.22244_22245delinsCT (TTN)	ENSP00000340554.6:p.Pro7415=
ENST00000359218.10:c.22043_22044delinsCT (TTN)	ENSP00000352154.5:p.Pro7348=
ENST00000342175.10:c.22244_22245delinsCT (TTN)	ENSP00000340554.6:p.Pro7415=
ENST00000342992.10:c.41159_41160delinsCT (TTN)	ENSP00000343764.6:p.Pro13720=
ENST00000359218.9:c.22043_22044delinsCT (TTN)	ENSP00000352154.5:p.Pro7348=
ENST00000460472.6:c.21668_21669delinsCT (TTN)	ENSP00000434586.1:p.Pro7223=
ENST00000589042.5:c.48863_48864delinsCT (TTN) MANE Select	ENSP00000467141.1:p.Pro16288=
ENST00000591111.5:c.43940_43941delinsCT (TTN)	ENSP00000465570.1:p.Pro14647=
ENST00000615779.4:c.43940_43941delinsCT (TTN)	ENSP00000483597.1:p.Pro14647=
NM_001256850.1:c.43940_43941delinsCT (TTN)	NP_001243779.1:p.Pro14647=
NM_001267550.2:c.48863_48864delinsCT (TTN) MANE Select	NP_001254479.2:p.Pro16288=
NM_003319.4:c.21668_21669delinsCT (TTN)	NP_003310.4:p.Pro7223=
NM_133378.4:c.41159_41160delinsCT (TTN)	NP_596869.4:p.Pro13720=
NM_133432.3:c.22043_22044delinsCT (TTN)	NP_597676.3:p.Pro7348=
NM_133437.4:c.22244_22245delinsCT (TTN)	NP_597681.4:p.Pro7415=
NR_038271.1:n.1398_1399delinsAG (TTN-AS1)
XM_011511729.1:c.47960_47961delinsCT (TTN)	XP_011510031.1:p.Pro15987=
XM_011511730.1:c.21854_21855delinsCT (TTN)	XP_011510032.1:p.Pro7285=
XM_011511731.1:c.21713_21714delinsCT (TTN)	XP_011510033.1:p.Pro7238=
XM_017004819.1:c.47756_47757delinsCT (TTN)	XP_016860308.1:p.Pro15919=
XM_017004820.1:c.43154_43155delinsCT (TTN)	XP_016860309.1:p.Pro14385=
XM_017004821.1:c.43151_43152delinsCT (TTN)	XP_016860310.1:p.Pro14384=
XM_017004822.1:c.40193_40194delinsCT (TTN)	XP_016860311.1:p.Pro13398=
XM_017004823.1:c.21809_21810delinsCT (TTN)	XP_016860312.1:p.Pro7270=
XM_024453094.1:c.43304_43305delinsCT (TTN)	XP_024308862.1:p.Pro14435=
XM_024453095.1:c.43301_43302delinsCT (TTN)	XP_024308863.1:p.Pro14434=
XM_024453096.1:c.42734_42735delinsCT (TTN)	XP_024308864.1:p.Pro14245=
XM_024453097.1:c.40076_40077delinsCT (TTN)	XP_024308865.1:p.Pro13359=
XM_024453098.1:c.39995_39996delinsCT (TTN)	XP_024308866.1:p.Pro13332=
XM_024453099.1:c.21758_21759delinsCT (TTN)	XP_024308867.1:p.Pro7253=
XM_024453100.1:c.11612_11613delinsCT (TTN)	XP_024308868.1:p.Pro3871=