Canonical Allele Identifier: CA349399928

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527509C>A , CM000664.2:g.178527509C>A	GRCh38
NC_000002.11:g.179392236C>A , CM000664.1:g.179392236C>A	GRCh37
NC_000002.10:g.179100482C>A	NCBI36
NG_011618.3:g.308294G>T , LRG_391:g.308294G>T
NG_051363.1:g.9683C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.107617G>T (TTN) MANE Select	NP_001254479.2:p.Gly35873Ter
ENST00000589042.5:c.107617G>T (TTN) MANE Select	ENSP00000467141.1:p.Gly35873Ter
NM_001256850.1:c.102694G>T (TTN)	NP_001243779.1:p.Gly34232Ter
NM_003319.4:c.80422G>T (TTN)	NP_003310.4:p.Gly26808Ter
NM_133378.4:c.99913G>T (TTN)	NP_596869.4:p.Gly33305Ter
NM_133432.3:c.80797G>T (TTN)	NP_597676.3:p.Gly26933Ter
NM_133437.4:c.80998G>T (TTN)	NP_597681.4:p.Gly27000Ter
NR_038271.1:n.446+3873C>A (TTN-AS1)
NR_038272.1:n.219+3873C>A (TTN-AS1)
ENST00000342175.10:c.80998G>T (TTN)	ENSP00000340554.6:p.Gly27000Ter
ENST00000342175.11:c.80998G>T (TTN)	ENSP00000340554.6:p.Gly27000Ter
ENST00000342992.10:c.99913G>T (TTN)	ENSP00000343764.6:p.Gly33305Ter
ENST00000342992.11:c.99913G>T (TTN)	ENSP00000343764.6:p.Gly33305Ter
ENST00000359218.10:c.80797G>T (TTN)	ENSP00000352154.5:p.Gly26933Ter
ENST00000359218.9:c.80797G>T (TTN)	ENSP00000352154.5:p.Gly26933Ter
ENST00000460472.6:c.80422G>T (TTN)	ENSP00000434586.1:p.Gly26808Ter
ENST00000591111.5:c.102694G>T (TTN)	ENSP00000465570.1:p.Gly34232Ter
ENST00000615779.4:c.102694G>T (TTN)	ENSP00000483597.1:p.Gly34232Ter
XM_011511729.1:c.106714G>T (TTN)	XP_011510031.1:p.Gly35572Ter
XM_011511730.1:c.80608G>T (TTN)	XP_011510032.1:p.Gly26870Ter
XM_011511731.1:c.80467G>T (TTN)	XP_011510033.1:p.Gly26823Ter
XM_017004819.1:c.106510G>T (TTN)	XP_016860308.1:p.Gly35504Ter
XM_017004820.1:c.101908G>T (TTN)	XP_016860309.1:p.Gly33970Ter
XM_017004821.1:c.101905G>T (TTN)	XP_016860310.1:p.Gly33969Ter
XM_017004822.1:c.98947G>T (TTN)	XP_016860311.1:p.Gly32983Ter
XM_017004823.1:c.80563G>T (TTN)	XP_016860312.1:p.Gly26855Ter
XM_024453094.1:c.102058G>T (TTN)	XP_024308862.1:p.Gly34020Ter
XM_024453095.1:c.102055G>T (TTN)	XP_024308863.1:p.Gly34019Ter
XM_024453096.1:c.101488G>T (TTN)	XP_024308864.1:p.Gly33830Ter
XM_024453097.1:c.98830G>T (TTN)	XP_024308865.1:p.Gly32944Ter
XM_024453098.1:c.98749G>T (TTN)	XP_024308866.1:p.Gly32917Ter
XM_024453099.1:c.80512G>T (TTN)	XP_024308867.1:p.Gly26838Ter
XM_024453100.1:c.70366G>T (TTN)	XP_024308868.1:p.Gly23456Ter