Canonical Allele Identifier: CA349465958

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546072G>A , CM000664.2:g.178546072G>A	GRCh38
NC_000002.11:g.179410799G>A , CM000664.1:g.179410799G>A	GRCh37
NC_000002.10:g.179119045G>A	NCBI36
NG_011618.3:g.289731C>T , LRG_391:g.289731C>T
NG_051363.1:g.28246G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.95164C>T (TTN) MANE Select	NP_001254479.2:p.Gln31722Ter
ENST00000589042.5:c.95164C>T (TTN) MANE Select	ENSP00000467141.1:p.Gln31722Ter
NM_001256850.1:c.90241C>T (TTN)	NP_001243779.1:p.Gln30081Ter
NM_003319.4:c.67969C>T (TTN)	NP_003310.4:p.Gln22657Ter
NM_133378.4:c.87460C>T (TTN)	NP_596869.4:p.Gln29154Ter
NM_133432.3:c.68344C>T (TTN)	NP_597676.3:p.Gln22782Ter
NM_133437.4:c.68545C>T (TTN)	NP_597681.4:p.Gln22849Ter
NR_038271.1:n.446+22436G>A (TTN-AS1)
NR_038272.1:n.2043+3711G>A (TTN-AS1)
ENST00000342175.10:c.68545C>T (TTN)	ENSP00000340554.6:p.Gln22849Ter
ENST00000342175.11:c.68545C>T (TTN)	ENSP00000340554.6:p.Gln22849Ter
ENST00000342992.10:c.87460C>T (TTN)	ENSP00000343764.6:p.Gln29154Ter
ENST00000342992.11:c.87460C>T (TTN)	ENSP00000343764.6:p.Gln29154Ter
ENST00000359218.10:c.68344C>T (TTN)	ENSP00000352154.5:p.Gln22782Ter
ENST00000359218.9:c.68344C>T (TTN)	ENSP00000352154.5:p.Gln22782Ter
ENST00000460472.6:c.67969C>T (TTN)	ENSP00000434586.1:p.Gln22657Ter
ENST00000591111.5:c.90241C>T (TTN)	ENSP00000465570.1:p.Gln30081Ter
ENST00000615779.4:c.90241C>T (TTN)	ENSP00000483597.1:p.Gln30081Ter
XM_011511729.1:c.94261C>T (TTN)	XP_011510031.1:p.Gln31421Ter
XM_011511730.1:c.68155C>T (TTN)	XP_011510032.1:p.Gln22719Ter
XM_011511731.1:c.68014C>T (TTN)	XP_011510033.1:p.Gln22672Ter
XM_017004819.1:c.94057C>T (TTN)	XP_016860308.1:p.Gln31353Ter
XM_017004820.1:c.89455C>T (TTN)	XP_016860309.1:p.Gln29819Ter
XM_017004821.1:c.89452C>T (TTN)	XP_016860310.1:p.Gln29818Ter
XM_017004822.1:c.86494C>T (TTN)	XP_016860311.1:p.Gln28832Ter
XM_017004823.1:c.68110C>T (TTN)	XP_016860312.1:p.Gln22704Ter
XM_024453094.1:c.89605C>T (TTN)	XP_024308862.1:p.Gln29869Ter
XM_024453095.1:c.89602C>T (TTN)	XP_024308863.1:p.Gln29868Ter
XM_024453096.1:c.89035C>T (TTN)	XP_024308864.1:p.Gln29679Ter
XM_024453097.1:c.86377C>T (TTN)	XP_024308865.1:p.Gln28793Ter
XM_024453098.1:c.86296C>T (TTN)	XP_024308866.1:p.Gln28766Ter
XM_024453099.1:c.68059C>T (TTN)	XP_024308867.1:p.Gln22687Ter
XM_024453100.1:c.57913C>T (TTN)	XP_024308868.1:p.Gln19305Ter