Canonical Allele Identifier: CA430237862

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178535218G>C , CM000664.2:g.178535218G>C	GRCh38
NC_000002.11:g.179399945G>C , CM000664.1:g.179399945G>C	GRCh37
NC_000002.10:g.179108191G>C	NCBI36
NG_011618.3:g.300585C>G , LRG_391:g.300585C>G
NG_051363.1:g.17392G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.101397C>G (TTN) MANE Select	NP_001254479.2:p.Thr33799=
ENST00000589042.5:c.101397C>G (TTN) MANE Select	ENSP00000467141.1:p.Thr33799=
NM_001256850.1:c.96474C>G (TTN)	NP_001243779.1:p.Thr32158=
NM_003319.4:c.74202C>G (TTN)	NP_003310.4:p.Thr24734=
NM_133378.4:c.93693C>G (TTN)	NP_596869.4:p.Thr31231=
NM_133432.3:c.74577C>G (TTN)	NP_597676.3:p.Thr24859=
NM_133437.4:c.74778C>G (TTN)	NP_597681.4:p.Thr24926=
NR_038271.1:n.446+11582G>C (TTN-AS1)
NR_038272.1:n.220-514G>C (TTN-AS1)
ENST00000342175.10:c.74778C>G (TTN)	ENSP00000340554.6:p.Thr24926=
ENST00000342175.11:c.74778C>G (TTN)	ENSP00000340554.6:p.Thr24926=
ENST00000342992.10:c.93693C>G (TTN)	ENSP00000343764.6:p.Thr31231=
ENST00000342992.11:c.93693C>G (TTN)	ENSP00000343764.6:p.Thr31231=
ENST00000359218.10:c.74577C>G (TTN)	ENSP00000352154.5:p.Thr24859=
ENST00000359218.9:c.74577C>G (TTN)	ENSP00000352154.5:p.Thr24859=
ENST00000460472.6:c.74202C>G (TTN)	ENSP00000434586.1:p.Thr24734=
ENST00000591111.5:c.96474C>G (TTN)	ENSP00000465570.1:p.Thr32158=
ENST00000615779.4:c.96474C>G (TTN)	ENSP00000483597.1:p.Thr32158=
XM_011511729.1:c.100494C>G (TTN)	XP_011510031.1:p.Thr33498=
XM_011511730.1:c.74388C>G (TTN)	XP_011510032.1:p.Thr24796=
XM_011511731.1:c.74247C>G (TTN)	XP_011510033.1:p.Thr24749=
XM_017004819.1:c.100290C>G (TTN)	XP_016860308.1:p.Thr33430=
XM_017004820.1:c.95688C>G (TTN)	XP_016860309.1:p.Thr31896=
XM_017004821.1:c.95685C>G (TTN)	XP_016860310.1:p.Thr31895=
XM_017004822.1:c.92727C>G (TTN)	XP_016860311.1:p.Thr30909=
XM_017004823.1:c.74343C>G (TTN)	XP_016860312.1:p.Thr24781=
XM_024453094.1:c.95838C>G (TTN)	XP_024308862.1:p.Thr31946=
XM_024453095.1:c.95835C>G (TTN)	XP_024308863.1:p.Thr31945=
XM_024453096.1:c.95268C>G (TTN)	XP_024308864.1:p.Thr31756=
XM_024453097.1:c.92610C>G (TTN)	XP_024308865.1:p.Thr30870=
XM_024453098.1:c.92529C>G (TTN)	XP_024308866.1:p.Thr30843=
XM_024453099.1:c.74292C>G (TTN)	XP_024308867.1:p.Thr24764=
XM_024453100.1:c.64146C>G (TTN)	XP_024308868.1:p.Thr21382=