Canonical Allele Identifier: CA349407116

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395279C>G (hg19) ; chr2:g.178530552C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530552C>G , CM000664.2:g.178530552C>G	GRCh38
NC_000002.11:g.179395279C>G , CM000664.1:g.179395279C>G	GRCh37
NC_000002.10:g.179103525C>G	NCBI36
NG_011618.3:g.305251G>C , LRG_391:g.305251G>C
NG_051363.1:g.12726C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98359G>C (TTN)	ENSP00000343764.6:p.Gly32787Arg
ENST00000342175.11:c.79444G>C (TTN)	ENSP00000340554.6:p.Gly26482Arg
ENST00000359218.10:c.79243G>C (TTN)	ENSP00000352154.5:p.Gly26415Arg
ENST00000342175.10:c.79444G>C (TTN)	ENSP00000340554.6:p.Gly26482Arg
ENST00000342992.10:c.98359G>C (TTN)	ENSP00000343764.6:p.Gly32787Arg
ENST00000359218.9:c.79243G>C (TTN)	ENSP00000352154.5:p.Gly26415Arg
ENST00000460472.6:c.78868G>C (TTN)	ENSP00000434586.1:p.Gly26290Arg
ENST00000589042.5:c.106063G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly35355Arg
ENST00000591111.5:c.101140G>C (TTN)	ENSP00000465570.1:p.Gly33714Arg
ENST00000615779.4:c.101140G>C (TTN)	ENSP00000483597.1:p.Gly33714Arg
NM_001256850.1:c.101140G>C (TTN)	NP_001243779.1:p.Gly33714Arg
NM_001267550.2:c.106063G>C (TTN) MANE Select	NP_001254479.2:p.Gly35355Arg
NM_003319.4:c.78868G>C (TTN)	NP_003310.4:p.Gly26290Arg
NM_133378.4:c.98359G>C (TTN)	NP_596869.4:p.Gly32787Arg
NM_133432.3:c.79243G>C (TTN)	NP_597676.3:p.Gly26415Arg
NM_133437.4:c.79444G>C (TTN)	NP_597681.4:p.Gly26482Arg
NR_038271.1:n.446+6916C>G (TTN-AS1)
NR_038272.1:n.220-5180C>G (TTN-AS1)
XM_011511729.1:c.105160G>C (TTN)	XP_011510031.1:p.Gly35054Arg
XM_011511730.1:c.79054G>C (TTN)	XP_011510032.1:p.Gly26352Arg
XM_011511731.1:c.78913G>C (TTN)	XP_011510033.1:p.Gly26305Arg
XM_017004819.1:c.104956G>C (TTN)	XP_016860308.1:p.Gly34986Arg
XM_017004820.1:c.100354G>C (TTN)	XP_016860309.1:p.Gly33452Arg
XM_017004821.1:c.100351G>C (TTN)	XP_016860310.1:p.Gly33451Arg
XM_017004822.1:c.97393G>C (TTN)	XP_016860311.1:p.Gly32465Arg
XM_017004823.1:c.79009G>C (TTN)	XP_016860312.1:p.Gly26337Arg
XM_024453094.1:c.100504G>C (TTN)	XP_024308862.1:p.Gly33502Arg
XM_024453095.1:c.100501G>C (TTN)	XP_024308863.1:p.Gly33501Arg
XM_024453096.1:c.99934G>C (TTN)	XP_024308864.1:p.Gly33312Arg
XM_024453097.1:c.97276G>C (TTN)	XP_024308865.1:p.Gly32426Arg
XM_024453098.1:c.97195G>C (TTN)	XP_024308866.1:p.Gly32399Arg
XM_024453099.1:c.78958G>C (TTN)	XP_024308867.1:p.Gly26320Arg
XM_024453100.1:c.68812G>C (TTN)	XP_024308868.1:p.Gly22938Arg