Canonical Allele Identifier: CA349426881

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179401790G>C (hg19) ; chr2:g.178537063G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178537063G>C , CM000664.2:g.178537063G>C	GRCh38
NC_000002.11:g.179401790G>C , CM000664.1:g.179401790G>C	GRCh37
NC_000002.10:g.179110036G>C	NCBI36
NG_011618.3:g.298740C>G , LRG_391:g.298740C>G
NG_051363.1:g.19237G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.92342C>G (TTN)	ENSP00000343764.6:p.Thr30781Arg
ENST00000342175.11:c.73427C>G (TTN)	ENSP00000340554.6:p.Thr24476Arg
ENST00000359218.10:c.73226C>G (TTN)	ENSP00000352154.5:p.Thr24409Arg
ENST00000342175.10:c.73427C>G (TTN)	ENSP00000340554.6:p.Thr24476Arg
ENST00000342992.10:c.92342C>G (TTN)	ENSP00000343764.6:p.Thr30781Arg
ENST00000359218.9:c.73226C>G (TTN)	ENSP00000352154.5:p.Thr24409Arg
ENST00000460472.6:c.72851C>G (TTN)	ENSP00000434586.1:p.Thr24284Arg
ENST00000589042.5:c.100046C>G (TTN) MANE Select	ENSP00000467141.1:p.Thr33349Arg
ENST00000591111.5:c.95123C>G (TTN)	ENSP00000465570.1:p.Thr31708Arg
ENST00000615779.4:c.95123C>G (TTN)	ENSP00000483597.1:p.Thr31708Arg
NM_001256850.1:c.95123C>G (TTN)	NP_001243779.1:p.Thr31708Arg
NM_001267550.2:c.100046C>G (TTN) MANE Select	NP_001254479.2:p.Thr33349Arg
NM_003319.4:c.72851C>G (TTN)	NP_003310.4:p.Thr24284Arg
NM_133378.4:c.92342C>G (TTN)	NP_596869.4:p.Thr30781Arg
NM_133432.3:c.73226C>G (TTN)	NP_597676.3:p.Thr24409Arg
NM_133437.4:c.73427C>G (TTN)	NP_597681.4:p.Thr24476Arg
NR_038271.1:n.446+13427G>C (TTN-AS1)
NR_038272.1:n.317-298G>C (TTN-AS1)
XM_011511729.1:c.99143C>G (TTN)	XP_011510031.1:p.Thr33048Arg
XM_011511730.1:c.73037C>G (TTN)	XP_011510032.1:p.Thr24346Arg
XM_011511731.1:c.72896C>G (TTN)	XP_011510033.1:p.Thr24299Arg
XM_017004819.1:c.98939C>G (TTN)	XP_016860308.1:p.Thr32980Arg
XM_017004820.1:c.94337C>G (TTN)	XP_016860309.1:p.Thr31446Arg
XM_017004821.1:c.94334C>G (TTN)	XP_016860310.1:p.Thr31445Arg
XM_017004822.1:c.91376C>G (TTN)	XP_016860311.1:p.Thr30459Arg
XM_017004823.1:c.72992C>G (TTN)	XP_016860312.1:p.Thr24331Arg
XM_024453094.1:c.94487C>G (TTN)	XP_024308862.1:p.Thr31496Arg
XM_024453095.1:c.94484C>G (TTN)	XP_024308863.1:p.Thr31495Arg
XM_024453096.1:c.93917C>G (TTN)	XP_024308864.1:p.Thr31306Arg
XM_024453097.1:c.91259C>G (TTN)	XP_024308865.1:p.Thr30420Arg
XM_024453098.1:c.91178C>G (TTN)	XP_024308866.1:p.Thr30393Arg
XM_024453099.1:c.72941C>G (TTN)	XP_024308867.1:p.Thr24314Arg
XM_024453100.1:c.62795C>G (TTN)	XP_024308868.1:p.Thr20932Arg