Canonical Allele Identifier: CA349474776

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178547160C>T , CM000664.2:g.178547160C>T	GRCh38
NC_000002.11:g.179411887C>T , CM000664.1:g.179411887C>T	GRCh37
NC_000002.10:g.179120133C>T	NCBI36
NG_011618.3:g.288643G>A , LRG_391:g.288643G>A
NG_051363.1:g.29334C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.94365G>A (TTN) MANE Select	NP_001254479.2:p.Trp31455Ter
ENST00000589042.5:c.94365G>A (TTN) MANE Select	ENSP00000467141.1:p.Trp31455Ter
NM_001256850.1:c.89442G>A (TTN)	NP_001243779.1:p.Trp29814Ter
NM_003319.4:c.67170G>A (TTN)	NP_003310.4:p.Trp22390Ter
NM_133378.4:c.86661G>A (TTN)	NP_596869.4:p.Trp28887Ter
NM_133432.3:c.67545G>A (TTN)	NP_597676.3:p.Trp22515Ter
NM_133437.4:c.67746G>A (TTN)	NP_597681.4:p.Trp22582Ter
NR_038271.1:n.446+23524C>T (TTN-AS1)
NR_038272.1:n.2043+4799C>T (TTN-AS1)
ENST00000342175.10:c.67746G>A (TTN)	ENSP00000340554.6:p.Trp22582Ter
ENST00000342175.11:c.67746G>A (TTN)	ENSP00000340554.6:p.Trp22582Ter
ENST00000342992.10:c.86661G>A (TTN)	ENSP00000343764.6:p.Trp28887Ter
ENST00000342992.11:c.86661G>A (TTN)	ENSP00000343764.6:p.Trp28887Ter
ENST00000359218.10:c.67545G>A (TTN)	ENSP00000352154.5:p.Trp22515Ter
ENST00000359218.9:c.67545G>A (TTN)	ENSP00000352154.5:p.Trp22515Ter
ENST00000460472.6:c.67170G>A (TTN)	ENSP00000434586.1:p.Trp22390Ter
ENST00000591111.5:c.89442G>A (TTN)	ENSP00000465570.1:p.Trp29814Ter
ENST00000615779.4:c.89442G>A (TTN)	ENSP00000483597.1:p.Trp29814Ter
XM_011511729.1:c.93462G>A (TTN)	XP_011510031.1:p.Trp31154Ter
XM_011511730.1:c.67356G>A (TTN)	XP_011510032.1:p.Trp22452Ter
XM_011511731.1:c.67215G>A (TTN)	XP_011510033.1:p.Trp22405Ter
XM_017004819.1:c.93258G>A (TTN)	XP_016860308.1:p.Trp31086Ter
XM_017004820.1:c.88656G>A (TTN)	XP_016860309.1:p.Trp29552Ter
XM_017004821.1:c.88653G>A (TTN)	XP_016860310.1:p.Trp29551Ter
XM_017004822.1:c.85695G>A (TTN)	XP_016860311.1:p.Trp28565Ter
XM_017004823.1:c.67311G>A (TTN)	XP_016860312.1:p.Trp22437Ter
XM_024453094.1:c.88806G>A (TTN)	XP_024308862.1:p.Trp29602Ter
XM_024453095.1:c.88803G>A (TTN)	XP_024308863.1:p.Trp29601Ter
XM_024453096.1:c.88236G>A (TTN)	XP_024308864.1:p.Trp29412Ter
XM_024453097.1:c.85578G>A (TTN)	XP_024308865.1:p.Trp28526Ter
XM_024453098.1:c.85497G>A (TTN)	XP_024308866.1:p.Trp28499Ter
XM_024453099.1:c.67260G>A (TTN)	XP_024308867.1:p.Trp22420Ter
XM_024453100.1:c.57114G>A (TTN)	XP_024308868.1:p.Trp19038Ter