Canonical Allele Identifier: CA349405385

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs2154132425
• MyVariant Identifiers: chr2:g.179394798C>G (hg19) ; chr2:g.178530071C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530071C>G , CM000664.2:g.178530071C>G	GRCh38
NC_000002.11:g.179394798C>G , CM000664.1:g.179394798C>G	GRCh37
NC_000002.10:g.179103044C>G	NCBI36
NG_011618.3:g.305732G>C , LRG_391:g.305732G>C
NG_051363.1:g.12245C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98716G>C (TTN)	ENSP00000343764.6:p.Gly32906Arg
ENST00000342175.11:c.79801G>C (TTN)	ENSP00000340554.6:p.Gly26601Arg
ENST00000359218.10:c.79600G>C (TTN)	ENSP00000352154.5:p.Gly26534Arg
ENST00000342175.10:c.79801G>C (TTN)	ENSP00000340554.6:p.Gly26601Arg
ENST00000342992.10:c.98716G>C (TTN)	ENSP00000343764.6:p.Gly32906Arg
ENST00000359218.9:c.79600G>C (TTN)	ENSP00000352154.5:p.Gly26534Arg
ENST00000460472.6:c.79225G>C (TTN)	ENSP00000434586.1:p.Gly26409Arg
ENST00000589042.5:c.106420G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly35474Arg
ENST00000591111.5:c.101497G>C (TTN)	ENSP00000465570.1:p.Gly33833Arg
ENST00000615779.4:c.101497G>C (TTN)	ENSP00000483597.1:p.Gly33833Arg
NM_001256850.1:c.101497G>C (TTN)	NP_001243779.1:p.Gly33833Arg
NM_001267550.2:c.106420G>C (TTN) MANE Select	NP_001254479.2:p.Gly35474Arg
NM_003319.4:c.79225G>C (TTN)	NP_003310.4:p.Gly26409Arg
NM_133378.4:c.98716G>C (TTN)	NP_596869.4:p.Gly32906Arg
NM_133432.3:c.79600G>C (TTN)	NP_597676.3:p.Gly26534Arg
NM_133437.4:c.79801G>C (TTN)	NP_597681.4:p.Gly26601Arg
NR_038271.1:n.446+6435C>G (TTN-AS1)
NR_038272.1:n.220-5661C>G (TTN-AS1)
XM_011511729.1:c.105517G>C (TTN)	XP_011510031.1:p.Gly35173Arg
XM_011511730.1:c.79411G>C (TTN)	XP_011510032.1:p.Gly26471Arg
XM_011511731.1:c.79270G>C (TTN)	XP_011510033.1:p.Gly26424Arg
XM_017004819.1:c.105313G>C (TTN)	XP_016860308.1:p.Gly35105Arg
XM_017004820.1:c.100711G>C (TTN)	XP_016860309.1:p.Gly33571Arg
XM_017004821.1:c.100708G>C (TTN)	XP_016860310.1:p.Gly33570Arg
XM_017004822.1:c.97750G>C (TTN)	XP_016860311.1:p.Gly32584Arg
XM_017004823.1:c.79366G>C (TTN)	XP_016860312.1:p.Gly26456Arg
XM_024453094.1:c.100861G>C (TTN)	XP_024308862.1:p.Gly33621Arg
XM_024453095.1:c.100858G>C (TTN)	XP_024308863.1:p.Gly33620Arg
XM_024453096.1:c.100291G>C (TTN)	XP_024308864.1:p.Gly33431Arg
XM_024453097.1:c.97633G>C (TTN)	XP_024308865.1:p.Gly32545Arg
XM_024453098.1:c.97552G>C (TTN)	XP_024308866.1:p.Gly32518Arg
XM_024453099.1:c.79315G>C (TTN)	XP_024308867.1:p.Gly26439Arg
XM_024453100.1:c.69169G>C (TTN)	XP_024308868.1:p.Gly23057Arg