Canonical Allele Identifier: CA349415472

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178533594C>A , CM000664.2:g.178533594C>A	GRCh38
NC_000002.11:g.179398321C>A , CM000664.1:g.179398321C>A	GRCh37
NC_000002.10:g.179106567C>A	NCBI36
NG_011618.3:g.302209G>T , LRG_391:g.302209G>T
NG_051363.1:g.15768C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.103021G>T (TTN) MANE Select	NP_001254479.2:p.Glu34341Ter
ENST00000589042.5:c.103021G>T (TTN) MANE Select	ENSP00000467141.1:p.Glu34341Ter
NM_001256850.1:c.98098G>T (TTN)	NP_001243779.1:p.Glu32700Ter
NM_003319.4:c.75826G>T (TTN)	NP_003310.4:p.Glu25276Ter
NM_133378.4:c.95317G>T (TTN)	NP_596869.4:p.Glu31773Ter
NM_133432.3:c.76201G>T (TTN)	NP_597676.3:p.Glu25401Ter
NM_133437.4:c.76402G>T (TTN)	NP_597681.4:p.Glu25468Ter
NR_038271.1:n.446+9958C>A (TTN-AS1)
NR_038272.1:n.220-2138C>A (TTN-AS1)
ENST00000342175.10:c.76402G>T (TTN)	ENSP00000340554.6:p.Glu25468Ter
ENST00000342175.11:c.76402G>T (TTN)	ENSP00000340554.6:p.Glu25468Ter
ENST00000342992.10:c.95317G>T (TTN)	ENSP00000343764.6:p.Glu31773Ter
ENST00000342992.11:c.95317G>T (TTN)	ENSP00000343764.6:p.Glu31773Ter
ENST00000359218.10:c.76201G>T (TTN)	ENSP00000352154.5:p.Glu25401Ter
ENST00000359218.9:c.76201G>T (TTN)	ENSP00000352154.5:p.Glu25401Ter
ENST00000460472.6:c.75826G>T (TTN)	ENSP00000434586.1:p.Glu25276Ter
ENST00000591111.5:c.98098G>T (TTN)	ENSP00000465570.1:p.Glu32700Ter
ENST00000615779.4:c.98098G>T (TTN)	ENSP00000483597.1:p.Glu32700Ter
XM_011511729.1:c.102118G>T (TTN)	XP_011510031.1:p.Glu34040Ter
XM_011511730.1:c.76012G>T (TTN)	XP_011510032.1:p.Glu25338Ter
XM_011511731.1:c.75871G>T (TTN)	XP_011510033.1:p.Glu25291Ter
XM_017004819.1:c.101914G>T (TTN)	XP_016860308.1:p.Glu33972Ter
XM_017004820.1:c.97312G>T (TTN)	XP_016860309.1:p.Glu32438Ter
XM_017004821.1:c.97309G>T (TTN)	XP_016860310.1:p.Glu32437Ter
XM_017004822.1:c.94351G>T (TTN)	XP_016860311.1:p.Glu31451Ter
XM_017004823.1:c.75967G>T (TTN)	XP_016860312.1:p.Glu25323Ter
XM_024453094.1:c.97462G>T (TTN)	XP_024308862.1:p.Glu32488Ter
XM_024453095.1:c.97459G>T (TTN)	XP_024308863.1:p.Glu32487Ter
XM_024453096.1:c.96892G>T (TTN)	XP_024308864.1:p.Glu32298Ter
XM_024453097.1:c.94234G>T (TTN)	XP_024308865.1:p.Glu31412Ter
XM_024453098.1:c.94153G>T (TTN)	XP_024308866.1:p.Glu31385Ter
XM_024453099.1:c.75916G>T (TTN)	XP_024308867.1:p.Glu25306Ter
XM_024453100.1:c.65770G>T (TTN)	XP_024308868.1:p.Glu21924Ter