Canonical Allele Identifier: CA349413554

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532850G>A , CM000664.2:g.178532850G>A	GRCh38
NC_000002.11:g.179397577G>A , CM000664.1:g.179397577G>A	GRCh37
NC_000002.10:g.179105823G>A	NCBI36
NG_011618.3:g.302953C>T , LRG_391:g.302953C>T
NG_051363.1:g.15024G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.103765C>T (TTN) MANE Select	NP_001254479.2:p.Gln34589Ter
ENST00000589042.5:c.103765C>T (TTN) MANE Select	ENSP00000467141.1:p.Gln34589Ter
NM_001256850.1:c.98842C>T (TTN)	NP_001243779.1:p.Gln32948Ter
NM_003319.4:c.76570C>T (TTN)	NP_003310.4:p.Gln25524Ter
NM_133378.4:c.96061C>T (TTN)	NP_596869.4:p.Gln32021Ter
NM_133432.3:c.76945C>T (TTN)	NP_597676.3:p.Gln25649Ter
NM_133437.4:c.77146C>T (TTN)	NP_597681.4:p.Gln25716Ter
NR_038271.1:n.446+9214G>A (TTN-AS1)
NR_038272.1:n.220-2882G>A (TTN-AS1)
ENST00000342175.10:c.77146C>T (TTN)	ENSP00000340554.6:p.Gln25716Ter
ENST00000342175.11:c.77146C>T (TTN)	ENSP00000340554.6:p.Gln25716Ter
ENST00000342992.10:c.96061C>T (TTN)	ENSP00000343764.6:p.Gln32021Ter
ENST00000342992.11:c.96061C>T (TTN)	ENSP00000343764.6:p.Gln32021Ter
ENST00000359218.10:c.76945C>T (TTN)	ENSP00000352154.5:p.Gln25649Ter
ENST00000359218.9:c.76945C>T (TTN)	ENSP00000352154.5:p.Gln25649Ter
ENST00000460472.6:c.76570C>T (TTN)	ENSP00000434586.1:p.Gln25524Ter
ENST00000591111.5:c.98842C>T (TTN)	ENSP00000465570.1:p.Gln32948Ter
ENST00000615779.4:c.98842C>T (TTN)	ENSP00000483597.1:p.Gln32948Ter
XM_011511729.1:c.102862C>T (TTN)	XP_011510031.1:p.Gln34288Ter
XM_011511730.1:c.76756C>T (TTN)	XP_011510032.1:p.Gln25586Ter
XM_011511731.1:c.76615C>T (TTN)	XP_011510033.1:p.Gln25539Ter
XM_017004819.1:c.102658C>T (TTN)	XP_016860308.1:p.Gln34220Ter
XM_017004820.1:c.98056C>T (TTN)	XP_016860309.1:p.Gln32686Ter
XM_017004821.1:c.98053C>T (TTN)	XP_016860310.1:p.Gln32685Ter
XM_017004822.1:c.95095C>T (TTN)	XP_016860311.1:p.Gln31699Ter
XM_017004823.1:c.76711C>T (TTN)	XP_016860312.1:p.Gln25571Ter
XM_024453094.1:c.98206C>T (TTN)	XP_024308862.1:p.Gln32736Ter
XM_024453095.1:c.98203C>T (TTN)	XP_024308863.1:p.Gln32735Ter
XM_024453096.1:c.97636C>T (TTN)	XP_024308864.1:p.Gln32546Ter
XM_024453097.1:c.94978C>T (TTN)	XP_024308865.1:p.Gln31660Ter
XM_024453098.1:c.94897C>T (TTN)	XP_024308866.1:p.Gln31633Ter
XM_024453099.1:c.76660C>T (TTN)	XP_024308867.1:p.Gln25554Ter
XM_024453100.1:c.66514C>T (TTN)	XP_024308868.1:p.Gln22172Ter