Canonical Allele Identifier: CA1310551177

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178618785C= , CM000664.2:g.178618785C=	GRCh38
NC_000002.11:g.179483512C= , CM000664.1:g.179483512C=	GRCh37
NC_000002.10:g.179191757C=	NCBI36
NG_011618.3:g.217018G= , LRG_391:g.217018G=
NG_051363.1:g.100959C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.39061G= (TTN)	ENSP00000343764.6:p.Val13021=
ENST00000342175.11:c.20146G= (TTN)	ENSP00000340554.6:p.Val6716=
ENST00000359218.10:c.19945G= (TTN)	ENSP00000352154.5:p.Val6649=
ENST00000342175.10:c.20146G= (TTN)	ENSP00000340554.6:p.Val6716=
ENST00000342992.10:c.39061G= (TTN)	ENSP00000343764.6:p.Val13021=
ENST00000359218.9:c.19945G= (TTN)	ENSP00000352154.5:p.Val6649=
ENST00000460472.6:c.19570G= (TTN)	ENSP00000434586.1:p.Val6524=
ENST00000589042.5:c.46765G= (TTN) MANE Select	ENSP00000467141.1:p.Val15589=
ENST00000591111.5:c.41842G= (TTN)	ENSP00000465570.1:p.Val13948=
ENST00000615779.4:c.41842G= (TTN)	ENSP00000483597.1:p.Val13948=
NM_001256850.1:c.41842G= (TTN)	NP_001243779.1:p.Val13948=
NM_001267550.2:c.46765G= (TTN) MANE Select	NP_001254479.2:p.Val15589=
NM_003319.4:c.19570G= (TTN)	NP_003310.4:p.Val6524=
NM_133378.4:c.39061G= (TTN)	NP_596869.4:p.Val13021=
NM_133432.3:c.19945G= (TTN)	NP_597676.3:p.Val6649=
NM_133437.4:c.20146G= (TTN)	NP_597681.4:p.Val6716=
NR_038271.1:n.1605-968C= (TTN-AS1)
XM_011511729.1:c.45862G= (TTN)	XP_011510031.1:p.Val15288=
XM_011511730.1:c.19756G= (TTN)	XP_011510032.1:p.Val6586=
XM_011511731.1:c.19615G= (TTN)	XP_011510033.1:p.Val6539=
XM_017004819.1:c.45658G= (TTN)	XP_016860308.1:p.Val15220=
XM_017004820.1:c.41056G= (TTN)	XP_016860309.1:p.Val13686=
XM_017004821.1:c.41053G= (TTN)	XP_016860310.1:p.Val13685=
XM_017004822.1:c.38095G= (TTN)	XP_016860311.1:p.Val12699=
XM_017004823.1:c.19711G= (TTN)	XP_016860312.1:p.Val6571=
XM_024453094.1:c.41206G= (TTN)	XP_024308862.1:p.Val13736=
XM_024453095.1:c.41203G= (TTN)	XP_024308863.1:p.Val13735=
XM_024453096.1:c.40636G= (TTN)	XP_024308864.1:p.Val13546=
XM_024453097.1:c.37978G= (TTN)	XP_024308865.1:p.Val12660=
XM_024453098.1:c.37897G= (TTN)	XP_024308866.1:p.Val12633=
XM_024453099.1:c.19660G= (TTN)	XP_024308867.1:p.Val6554=
XM_024453100.1:c.9514G= (TTN)	XP_024308868.1:p.Val3172=