Canonical Allele Identifier: CA349534100

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178557446A>T , CM000664.2:g.178557446A>T	GRCh38
NC_000002.11:g.179422173A>T , CM000664.1:g.179422173A>T	GRCh37
NC_000002.10:g.179130419A>T	NCBI36
NG_011618.3:g.278357T>A , LRG_391:g.278357T>A
NG_051363.1:g.39620A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.87816T>A (TTN) MANE Select	NP_001254479.2:p.Tyr29272Ter
ENST00000589042.5:c.87816T>A (TTN) MANE Select	ENSP00000467141.1:p.Tyr29272Ter
NM_001256850.1:c.82893T>A (TTN)	NP_001243779.1:p.Tyr27631Ter
NM_003319.4:c.60621T>A (TTN)	NP_003310.4:p.Tyr20207Ter
NM_133378.4:c.80112T>A (TTN)	NP_596869.4:p.Tyr26704Ter
NM_133432.3:c.60996T>A (TTN)	NP_597676.3:p.Tyr20332Ter
NM_133437.4:c.61197T>A (TTN)	NP_597681.4:p.Tyr20399Ter
NR_038271.1:n.447-13854A>T (TTN-AS1)
NR_038272.1:n.2043+15085A>T (TTN-AS1)
ENST00000342175.10:c.61197T>A (TTN)	ENSP00000340554.6:p.Tyr20399Ter
ENST00000342175.11:c.61197T>A (TTN)	ENSP00000340554.6:p.Tyr20399Ter
ENST00000342992.10:c.80112T>A (TTN)	ENSP00000343764.6:p.Tyr26704Ter
ENST00000342992.11:c.80112T>A (TTN)	ENSP00000343764.6:p.Tyr26704Ter
ENST00000359218.10:c.60996T>A (TTN)	ENSP00000352154.5:p.Tyr20332Ter
ENST00000359218.9:c.60996T>A (TTN)	ENSP00000352154.5:p.Tyr20332Ter
ENST00000460472.6:c.60621T>A (TTN)	ENSP00000434586.1:p.Tyr20207Ter
ENST00000591111.5:c.82893T>A (TTN)	ENSP00000465570.1:p.Tyr27631Ter
ENST00000615779.4:c.82893T>A (TTN)	ENSP00000483597.1:p.Tyr27631Ter
XM_011511729.1:c.86913T>A (TTN)	XP_011510031.1:p.Tyr28971Ter
XM_011511730.1:c.60807T>A (TTN)	XP_011510032.1:p.Tyr20269Ter
XM_011511731.1:c.60666T>A (TTN)	XP_011510033.1:p.Tyr20222Ter
XM_017004819.1:c.86709T>A (TTN)	XP_016860308.1:p.Tyr28903Ter
XM_017004820.1:c.82107T>A (TTN)	XP_016860309.1:p.Tyr27369Ter
XM_017004821.1:c.82104T>A (TTN)	XP_016860310.1:p.Tyr27368Ter
XM_017004822.1:c.79146T>A (TTN)	XP_016860311.1:p.Tyr26382Ter
XM_017004823.1:c.60762T>A (TTN)	XP_016860312.1:p.Tyr20254Ter
XM_024453094.1:c.82257T>A (TTN)	XP_024308862.1:p.Tyr27419Ter
XM_024453095.1:c.82254T>A (TTN)	XP_024308863.1:p.Tyr27418Ter
XM_024453096.1:c.81687T>A (TTN)	XP_024308864.1:p.Tyr27229Ter
XM_024453097.1:c.79029T>A (TTN)	XP_024308865.1:p.Tyr26343Ter
XM_024453098.1:c.78948T>A (TTN)	XP_024308866.1:p.Tyr26316Ter
XM_024453099.1:c.60711T>A (TTN)	XP_024308867.1:p.Tyr20237Ter
XM_024453100.1:c.50565T>A (TTN)	XP_024308868.1:p.Tyr16855Ter