Canonical Allele Identifier: CA430273780

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178612996T>C , CM000664.2:g.178612996T>C	GRCh38
NC_000002.11:g.179477723T>C , CM000664.1:g.179477723T>C	GRCh37
NC_000002.10:g.179185968T>C	NCBI36
NG_011618.3:g.222807A>G , LRG_391:g.222807A>G
NG_051363.1:g.95170T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.49725A>G (TTN) MANE Select	NP_001254479.2:p.Pro16575=
ENST00000589042.5:c.49725A>G (TTN) MANE Select	ENSP00000467141.1:p.Pro16575=
NM_001256850.1:c.44802A>G (TTN)	NP_001243779.1:p.Pro14934=
NM_003319.4:c.22530A>G (TTN)	NP_003310.4:p.Pro7510=
NM_133378.4:c.42021A>G (TTN)	NP_596869.4:p.Pro14007=
NM_133432.3:c.22905A>G (TTN)	NP_597676.3:p.Pro7635=
NM_133437.4:c.23106A>G (TTN)	NP_597681.4:p.Pro7702=
NR_038271.1:n.783-1039T>C (TTN-AS1)
ENST00000342175.10:c.23106A>G (TTN)	ENSP00000340554.6:p.Pro7702=
ENST00000342175.11:c.23106A>G (TTN)	ENSP00000340554.6:p.Pro7702=
ENST00000342992.10:c.42021A>G (TTN)	ENSP00000343764.6:p.Pro14007=
ENST00000342992.11:c.42021A>G (TTN)	ENSP00000343764.6:p.Pro14007=
ENST00000359218.10:c.22905A>G (TTN)	ENSP00000352154.5:p.Pro7635=
ENST00000359218.9:c.22905A>G (TTN)	ENSP00000352154.5:p.Pro7635=
ENST00000460472.6:c.22530A>G (TTN)	ENSP00000434586.1:p.Pro7510=
ENST00000591111.5:c.44802A>G (TTN)	ENSP00000465570.1:p.Pro14934=
ENST00000615779.4:c.44802A>G (TTN)	ENSP00000483597.1:p.Pro14934=
XM_011511729.1:c.48822A>G (TTN)	XP_011510031.1:p.Pro16274=
XM_011511730.1:c.22716A>G (TTN)	XP_011510032.1:p.Pro7572=
XM_011511731.1:c.22575A>G (TTN)	XP_011510033.1:p.Pro7525=
XM_017004819.1:c.48618A>G (TTN)	XP_016860308.1:p.Pro16206=
XM_017004820.1:c.44016A>G (TTN)	XP_016860309.1:p.Pro14672=
XM_017004821.1:c.44013A>G (TTN)	XP_016860310.1:p.Pro14671=
XM_017004822.1:c.41055A>G (TTN)	XP_016860311.1:p.Pro13685=
XM_017004823.1:c.22671A>G (TTN)	XP_016860312.1:p.Pro7557=
XM_024453094.1:c.44166A>G (TTN)	XP_024308862.1:p.Pro14722=
XM_024453095.1:c.44163A>G (TTN)	XP_024308863.1:p.Pro14721=
XM_024453096.1:c.43596A>G (TTN)	XP_024308864.1:p.Pro14532=
XM_024453097.1:c.40938A>G (TTN)	XP_024308865.1:p.Pro13646=
XM_024453098.1:c.40857A>G (TTN)	XP_024308866.1:p.Pro13619=
XM_024453099.1:c.22620A>G (TTN)	XP_024308867.1:p.Pro7540=
XM_024453100.1:c.12474A>G (TTN)	XP_024308868.1:p.Pro4158=