Canonical Allele Identifier: CA349419783

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178534887C>A , CM000664.2:g.178534887C>A	GRCh38
NC_000002.11:g.179399614C>A , CM000664.1:g.179399614C>A	GRCh37
NC_000002.10:g.179107860C>A	NCBI36
NG_011618.3:g.300916G>T , LRG_391:g.300916G>T
NG_051363.1:g.17061C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.101728G>T (TTN) MANE Select	NP_001254479.2:p.Glu33910Ter
ENST00000589042.5:c.101728G>T (TTN) MANE Select	ENSP00000467141.1:p.Glu33910Ter
NM_001256850.1:c.96805G>T (TTN)	NP_001243779.1:p.Glu32269Ter
NM_003319.4:c.74533G>T (TTN)	NP_003310.4:p.Glu24845Ter
NM_133378.4:c.94024G>T (TTN)	NP_596869.4:p.Glu31342Ter
NM_133432.3:c.74908G>T (TTN)	NP_597676.3:p.Glu24970Ter
NM_133437.4:c.75109G>T (TTN)	NP_597681.4:p.Glu25037Ter
NR_038271.1:n.446+11251C>A (TTN-AS1)
NR_038272.1:n.220-845C>A (TTN-AS1)
ENST00000342175.10:c.75109G>T (TTN)	ENSP00000340554.6:p.Glu25037Ter
ENST00000342175.11:c.75109G>T (TTN)	ENSP00000340554.6:p.Glu25037Ter
ENST00000342992.10:c.94024G>T (TTN)	ENSP00000343764.6:p.Glu31342Ter
ENST00000342992.11:c.94024G>T (TTN)	ENSP00000343764.6:p.Glu31342Ter
ENST00000359218.10:c.74908G>T (TTN)	ENSP00000352154.5:p.Glu24970Ter
ENST00000359218.9:c.74908G>T (TTN)	ENSP00000352154.5:p.Glu24970Ter
ENST00000460472.6:c.74533G>T (TTN)	ENSP00000434586.1:p.Glu24845Ter
ENST00000591111.5:c.96805G>T (TTN)	ENSP00000465570.1:p.Glu32269Ter
ENST00000615779.4:c.96805G>T (TTN)	ENSP00000483597.1:p.Glu32269Ter
XM_011511729.1:c.100825G>T (TTN)	XP_011510031.1:p.Glu33609Ter
XM_011511730.1:c.74719G>T (TTN)	XP_011510032.1:p.Glu24907Ter
XM_011511731.1:c.74578G>T (TTN)	XP_011510033.1:p.Glu24860Ter
XM_017004819.1:c.100621G>T (TTN)	XP_016860308.1:p.Glu33541Ter
XM_017004820.1:c.96019G>T (TTN)	XP_016860309.1:p.Glu32007Ter
XM_017004821.1:c.96016G>T (TTN)	XP_016860310.1:p.Glu32006Ter
XM_017004822.1:c.93058G>T (TTN)	XP_016860311.1:p.Glu31020Ter
XM_017004823.1:c.74674G>T (TTN)	XP_016860312.1:p.Glu24892Ter
XM_024453094.1:c.96169G>T (TTN)	XP_024308862.1:p.Glu32057Ter
XM_024453095.1:c.96166G>T (TTN)	XP_024308863.1:p.Glu32056Ter
XM_024453096.1:c.95599G>T (TTN)	XP_024308864.1:p.Glu31867Ter
XM_024453097.1:c.92941G>T (TTN)	XP_024308865.1:p.Glu30981Ter
XM_024453098.1:c.92860G>T (TTN)	XP_024308866.1:p.Glu30954Ter
XM_024453099.1:c.74623G>T (TTN)	XP_024308867.1:p.Glu24875Ter
XM_024453100.1:c.64477G>T (TTN)	XP_024308868.1:p.Glu21493Ter