Canonical Allele Identifier: CA1985868

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178535083T>C , CM000664.2:g.178535083T>C	GRCh38
NC_000002.11:g.179399810T>C , CM000664.1:g.179399810T>C	GRCh37
NC_000002.10:g.179108056T>C	NCBI36
NG_011618.3:g.300720A>G , LRG_391:g.300720A>G
NG_051363.1:g.17257T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.101532A>G (TTN) MANE Select	NP_001254479.2:p.Thr33844=
ENST00000589042.5:c.101532A>G (TTN) MANE Select	ENSP00000467141.1:p.Thr33844=
NM_001256850.1:c.96609A>G (TTN)	NP_001243779.1:p.Thr32203=
NM_003319.4:c.74337A>G (TTN)	NP_003310.4:p.Thr24779=
NM_133378.4:c.93828A>G (TTN)	NP_596869.4:p.Thr31276=
NM_133432.3:c.74712A>G (TTN)	NP_597676.3:p.Thr24904=
NM_133437.4:c.74913A>G (TTN)	NP_597681.4:p.Thr24971=
NR_038271.1:n.446+11447T>C (TTN-AS1)
NR_038272.1:n.220-649T>C (TTN-AS1)
ENST00000342175.10:c.74913A>G (TTN)	ENSP00000340554.6:p.Thr24971=
ENST00000342175.11:c.74913A>G (TTN)	ENSP00000340554.6:p.Thr24971=
ENST00000342992.10:c.93828A>G (TTN)	ENSP00000343764.6:p.Thr31276=
ENST00000342992.11:c.93828A>G (TTN)	ENSP00000343764.6:p.Thr31276=
ENST00000359218.10:c.74712A>G (TTN)	ENSP00000352154.5:p.Thr24904=
ENST00000359218.9:c.74712A>G (TTN)	ENSP00000352154.5:p.Thr24904=
ENST00000460472.6:c.74337A>G (TTN)	ENSP00000434586.1:p.Thr24779=
ENST00000591111.5:c.96609A>G (TTN)	ENSP00000465570.1:p.Thr32203=
ENST00000615779.4:c.96609A>G (TTN)	ENSP00000483597.1:p.Thr32203=
XM_011511729.1:c.100629A>G (TTN)	XP_011510031.1:p.Thr33543=
XM_011511730.1:c.74523A>G (TTN)	XP_011510032.1:p.Thr24841=
XM_011511731.1:c.74382A>G (TTN)	XP_011510033.1:p.Thr24794=
XM_017004819.1:c.100425A>G (TTN)	XP_016860308.1:p.Thr33475=
XM_017004820.1:c.95823A>G (TTN)	XP_016860309.1:p.Thr31941=
XM_017004821.1:c.95820A>G (TTN)	XP_016860310.1:p.Thr31940=
XM_017004822.1:c.92862A>G (TTN)	XP_016860311.1:p.Thr30954=
XM_017004823.1:c.74478A>G (TTN)	XP_016860312.1:p.Thr24826=
XM_024453094.1:c.95973A>G (TTN)	XP_024308862.1:p.Thr31991=
XM_024453095.1:c.95970A>G (TTN)	XP_024308863.1:p.Thr31990=
XM_024453096.1:c.95403A>G (TTN)	XP_024308864.1:p.Thr31801=
XM_024453097.1:c.92745A>G (TTN)	XP_024308865.1:p.Thr30915=
XM_024453098.1:c.92664A>G (TTN)	XP_024308866.1:p.Thr30888=
XM_024453099.1:c.74427A>G (TTN)	XP_024308867.1:p.Thr24809=
XM_024453100.1:c.64281A>G (TTN)	XP_024308868.1:p.Thr21427=