Canonical Allele Identifier: CA284291

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532039C>T , CM000664.2:g.178532039C>T	GRCh38
NC_000002.11:g.179396766C>T , CM000664.1:g.179396766C>T	GRCh37
NC_000002.10:g.179105012C>T	NCBI36
NG_011618.3:g.303764G>A , LRG_391:g.303764G>A
NG_051363.1:g.14213C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96872G>A (TTN)	ENSP00000343764.6:p.Arg32291Gln
ENST00000342175.11:c.77957G>A (TTN)	ENSP00000340554.6:p.Arg25986Gln
ENST00000359218.10:c.77756G>A (TTN)	ENSP00000352154.5:p.Arg25919Gln
ENST00000342175.10:c.77957G>A (TTN)	ENSP00000340554.6:p.Arg25986Gln
ENST00000342992.10:c.96872G>A (TTN)	ENSP00000343764.6:p.Arg32291Gln
ENST00000359218.9:c.77756G>A (TTN)	ENSP00000352154.5:p.Arg25919Gln
ENST00000460472.6:c.77381G>A (TTN)	ENSP00000434586.1:p.Arg25794Gln
ENST00000589042.5:c.104576G>A (TTN) MANE Select	ENSP00000467141.1:p.Arg34859Gln
ENST00000591111.5:c.99653G>A (TTN)	ENSP00000465570.1:p.Arg33218Gln
ENST00000615779.4:c.99653G>A (TTN)	ENSP00000483597.1:p.Arg33218Gln
NM_001256850.1:c.99653G>A (TTN)	NP_001243779.1:p.Arg33218Gln
NM_001267550.2:c.104576G>A (TTN) MANE Select	NP_001254479.2:p.Arg34859Gln
NM_003319.4:c.77381G>A (TTN)	NP_003310.4:p.Arg25794Gln
NM_133378.4:c.96872G>A (TTN)	NP_596869.4:p.Arg32291Gln
NM_133432.3:c.77756G>A (TTN)	NP_597676.3:p.Arg25919Gln
NM_133437.4:c.77957G>A (TTN)	NP_597681.4:p.Arg25986Gln
NR_038271.1:n.446+8403C>T (TTN-AS1)
NR_038272.1:n.220-3693C>T (TTN-AS1)
XM_011511729.1:c.103673G>A (TTN)	XP_011510031.1:p.Arg34558Gln
XM_011511730.1:c.77567G>A (TTN)	XP_011510032.1:p.Arg25856Gln
XM_011511731.1:c.77426G>A (TTN)	XP_011510033.1:p.Arg25809Gln
XM_017004819.1:c.103469G>A (TTN)	XP_016860308.1:p.Arg34490Gln
XM_017004820.1:c.98867G>A (TTN)	XP_016860309.1:p.Arg32956Gln
XM_017004821.1:c.98864G>A (TTN)	XP_016860310.1:p.Arg32955Gln
XM_017004822.1:c.95906G>A (TTN)	XP_016860311.1:p.Arg31969Gln
XM_017004823.1:c.77522G>A (TTN)	XP_016860312.1:p.Arg25841Gln
XM_024453094.1:c.99017G>A (TTN)	XP_024308862.1:p.Arg33006Gln
XM_024453095.1:c.99014G>A (TTN)	XP_024308863.1:p.Arg33005Gln
XM_024453096.1:c.98447G>A (TTN)	XP_024308864.1:p.Arg32816Gln
XM_024453097.1:c.95789G>A (TTN)	XP_024308865.1:p.Arg31930Gln
XM_024453098.1:c.95708G>A (TTN)	XP_024308866.1:p.Arg31903Gln
XM_024453099.1:c.77471G>A (TTN)	XP_024308867.1:p.Arg25824Gln
XM_024453100.1:c.67325G>A (TTN)	XP_024308868.1:p.Arg22442Gln