Canonical Allele Identifier: CA349486046

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178548289G>A , CM000664.2:g.178548289G>A	GRCh38
NC_000002.11:g.179413016G>A , CM000664.1:g.179413016G>A	GRCh37
NC_000002.10:g.179121262G>A	NCBI36
NG_011618.3:g.287514C>T , LRG_391:g.287514C>T
NG_051363.1:g.30463G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.93337C>T (TTN) MANE Select	NP_001254479.2:p.Gln31113Ter
ENST00000589042.5:c.93337C>T (TTN) MANE Select	ENSP00000467141.1:p.Gln31113Ter
NM_001256850.1:c.88414C>T (TTN)	NP_001243779.1:p.Gln29472Ter
NM_003319.4:c.66142C>T (TTN)	NP_003310.4:p.Gln22048Ter
NM_133378.4:c.85633C>T (TTN)	NP_596869.4:p.Gln28545Ter
NM_133432.3:c.66517C>T (TTN)	NP_597676.3:p.Gln22173Ter
NM_133437.4:c.66718C>T (TTN)	NP_597681.4:p.Gln22240Ter
NR_038271.1:n.447-23011G>A (TTN-AS1)
NR_038272.1:n.2043+5928G>A (TTN-AS1)
ENST00000342175.10:c.66718C>T (TTN)	ENSP00000340554.6:p.Gln22240Ter
ENST00000342175.11:c.66718C>T (TTN)	ENSP00000340554.6:p.Gln22240Ter
ENST00000342992.10:c.85633C>T (TTN)	ENSP00000343764.6:p.Gln28545Ter
ENST00000342992.11:c.85633C>T (TTN)	ENSP00000343764.6:p.Gln28545Ter
ENST00000359218.10:c.66517C>T (TTN)	ENSP00000352154.5:p.Gln22173Ter
ENST00000359218.9:c.66517C>T (TTN)	ENSP00000352154.5:p.Gln22173Ter
ENST00000460472.6:c.66142C>T (TTN)	ENSP00000434586.1:p.Gln22048Ter
ENST00000591111.5:c.88414C>T (TTN)	ENSP00000465570.1:p.Gln29472Ter
ENST00000615779.4:c.88414C>T (TTN)	ENSP00000483597.1:p.Gln29472Ter
XM_011511729.1:c.92434C>T (TTN)	XP_011510031.1:p.Gln30812Ter
XM_011511730.1:c.66328C>T (TTN)	XP_011510032.1:p.Gln22110Ter
XM_011511731.1:c.66187C>T (TTN)	XP_011510033.1:p.Gln22063Ter
XM_017004819.1:c.92230C>T (TTN)	XP_016860308.1:p.Gln30744Ter
XM_017004820.1:c.87628C>T (TTN)	XP_016860309.1:p.Gln29210Ter
XM_017004821.1:c.87625C>T (TTN)	XP_016860310.1:p.Gln29209Ter
XM_017004822.1:c.84667C>T (TTN)	XP_016860311.1:p.Gln28223Ter
XM_017004823.1:c.66283C>T (TTN)	XP_016860312.1:p.Gln22095Ter
XM_024453094.1:c.87778C>T (TTN)	XP_024308862.1:p.Gln29260Ter
XM_024453095.1:c.87775C>T (TTN)	XP_024308863.1:p.Gln29259Ter
XM_024453096.1:c.87208C>T (TTN)	XP_024308864.1:p.Gln29070Ter
XM_024453097.1:c.84550C>T (TTN)	XP_024308865.1:p.Gln28184Ter
XM_024453098.1:c.84469C>T (TTN)	XP_024308866.1:p.Gln28157Ter
XM_024453099.1:c.66232C>T (TTN)	XP_024308867.1:p.Gln22078Ter
XM_024453100.1:c.56086C>T (TTN)	XP_024308868.1:p.Gln18696Ter