Canonical Allele Identifier: CA1310540724

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178593560A>G , CM000664.2:g.178593560A>G	GRCh38
NC_000002.11:g.179458287A>G , CM000664.1:g.179458287A>G	GRCh37
NC_000002.10:g.179166533A>G	NCBI36
NG_011618.3:g.242243T>C , LRG_391:g.242243T>C
NG_051363.1:g.75734A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.58732+8T>C (TTN) MANE Select	NP_001254479.2:n.58732+8T>C
ENST00000589042.5:c.58732+8T>C (TTN) MANE Select	ENSP00000467141.1:n.58732+8T>C
NM_001256850.1:c.53809+8T>C (TTN)	NP_001243779.1:n.53809+8T>C
NM_003319.4:c.31537+8T>C (TTN)	NP_003310.4:n.31537+8T>C
NM_133378.4:c.51028+8T>C (TTN)	NP_596869.4:n.51028+8T>C
NM_133432.3:c.31912+8T>C (TTN)	NP_597676.3:n.31912+8T>C
NM_133437.4:c.32113+8T>C (TTN)	NP_597681.4:n.32113+8T>C
NR_038271.1:n.597-4036A>G (TTN-AS1)
NR_038272.1:n.3364+2246A>G (TTN-AS1)
ENST00000342175.10:c.32113+8T>C (TTN)	ENSP00000340554.6:n.32113+8T>C
ENST00000342175.11:c.32113+8T>C (TTN)	ENSP00000340554.6:n.32113+8T>C
ENST00000342992.10:c.51028+8T>C (TTN)	ENSP00000343764.6:n.51028+8T>C
ENST00000342992.11:c.51028+8T>C (TTN)	ENSP00000343764.6:n.51028+8T>C
ENST00000359218.10:c.31912+8T>C (TTN)	ENSP00000352154.5:n.31912+8T>C
ENST00000359218.9:c.31912+8T>C (TTN)	ENSP00000352154.5:n.31912+8T>C
ENST00000460472.6:c.31537+8T>C (TTN)	ENSP00000434586.1:n.31537+8T>C
ENST00000591111.5:c.53809+8T>C (TTN)	ENSP00000465570.1:n.53809+8T>C
ENST00000615779.4:c.53809+8T>C (TTN)	ENSP00000483597.1:n.53809+8T>C
XM_011511729.1:c.57829+8T>C (TTN)	XP_011510031.1:n.57829+8T>C
XM_011511730.1:c.31723+8T>C (TTN)	XP_011510032.1:n.31723+8T>C
XM_011511731.1:c.31582+8T>C (TTN)	XP_011510033.1:n.31582+8T>C
XM_017004819.1:c.57625+8T>C (TTN)	XP_016860308.1:n.57625+8T>C
XM_017004820.1:c.53023+8T>C (TTN)	XP_016860309.1:n.53023+8T>C
XM_017004821.1:c.53020+8T>C (TTN)	XP_016860310.1:n.53020+8T>C
XM_017004822.1:c.50062+8T>C (TTN)	XP_016860311.1:n.50062+8T>C
XM_017004823.1:c.31678+8T>C (TTN)	XP_016860312.1:n.31678+8T>C
XM_024453094.1:c.53173+8T>C (TTN)	XP_024308862.1:n.53173+8T>C
XM_024453095.1:c.53170+8T>C (TTN)	XP_024308863.1:n.53170+8T>C
XM_024453096.1:c.52603+8T>C (TTN)	XP_024308864.1:n.52603+8T>C
XM_024453097.1:c.49945+8T>C (TTN)	XP_024308865.1:n.49945+8T>C
XM_024453098.1:c.49864+8T>C (TTN)	XP_024308866.1:n.49864+8T>C
XM_024453099.1:c.31627+8T>C (TTN)	XP_024308867.1:n.31627+8T>C
XM_024453100.1:c.21481+8T>C (TTN)	XP_024308868.1:n.21481+8T>C