Canonical Allele Identifier: CA349622238

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618747C>T , CM000664.2:g.178618747C>T	GRCh38
NC_000002.11:g.179483474C>T , CM000664.1:g.179483474C>T	GRCh37
NC_000002.10:g.179191719C>T	NCBI36
NG_011618.3:g.217056G>A , LRG_391:g.217056G>A
NG_051363.1:g.100921C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.46803G>A (TTN) MANE Select	NP_001254479.2:p.Trp15601Ter
ENST00000589042.5:c.46803G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp15601Ter
NM_001256850.1:c.41880G>A (TTN)	NP_001243779.1:p.Trp13960Ter
NM_003319.4:c.19608G>A (TTN)	NP_003310.4:p.Trp6536Ter
NM_133378.4:c.39099G>A (TTN)	NP_596869.4:p.Trp13033Ter
NM_133432.3:c.19983G>A (TTN)	NP_597676.3:p.Trp6661Ter
NM_133437.4:c.20184G>A (TTN)	NP_597681.4:p.Trp6728Ter
NR_038271.1:n.1605-1006C>T (TTN-AS1)
ENST00000342175.10:c.20184G>A (TTN)	ENSP00000340554.6:p.Trp6728Ter
ENST00000342175.11:c.20184G>A (TTN)	ENSP00000340554.6:p.Trp6728Ter
ENST00000342992.10:c.39099G>A (TTN)	ENSP00000343764.6:p.Trp13033Ter
ENST00000342992.11:c.39099G>A (TTN)	ENSP00000343764.6:p.Trp13033Ter
ENST00000359218.10:c.19983G>A (TTN)	ENSP00000352154.5:p.Trp6661Ter
ENST00000359218.9:c.19983G>A (TTN)	ENSP00000352154.5:p.Trp6661Ter
ENST00000460472.6:c.19608G>A (TTN)	ENSP00000434586.1:p.Trp6536Ter
ENST00000591111.5:c.41880G>A (TTN)	ENSP00000465570.1:p.Trp13960Ter
ENST00000615779.4:c.41880G>A (TTN)	ENSP00000483597.1:p.Trp13960Ter
XM_011511729.1:c.45900G>A (TTN)	XP_011510031.1:p.Trp15300Ter
XM_011511730.1:c.19794G>A (TTN)	XP_011510032.1:p.Trp6598Ter
XM_011511731.1:c.19653G>A (TTN)	XP_011510033.1:p.Trp6551Ter
XM_017004819.1:c.45696G>A (TTN)	XP_016860308.1:p.Trp15232Ter
XM_017004820.1:c.41094G>A (TTN)	XP_016860309.1:p.Trp13698Ter
XM_017004821.1:c.41091G>A (TTN)	XP_016860310.1:p.Trp13697Ter
XM_017004822.1:c.38133G>A (TTN)	XP_016860311.1:p.Trp12711Ter
XM_017004823.1:c.19749G>A (TTN)	XP_016860312.1:p.Trp6583Ter
XM_024453094.1:c.41244G>A (TTN)	XP_024308862.1:p.Trp13748Ter
XM_024453095.1:c.41241G>A (TTN)	XP_024308863.1:p.Trp13747Ter
XM_024453096.1:c.40674G>A (TTN)	XP_024308864.1:p.Trp13558Ter
XM_024453097.1:c.38016G>A (TTN)	XP_024308865.1:p.Trp12672Ter
XM_024453098.1:c.37935G>A (TTN)	XP_024308866.1:p.Trp12645Ter
XM_024453099.1:c.19698G>A (TTN)	XP_024308867.1:p.Trp6566Ter
XM_024453100.1:c.9552G>A (TTN)	XP_024308868.1:p.Trp3184Ter