Canonical Allele Identifier: CA349425413

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1318771244
• MyVariant Identifiers: chr2:g.179400900G>C (hg19) ; chr2:g.178536173G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178536173G>C , CM000664.2:g.178536173G>C	GRCh38
NC_000002.11:g.179400900G>C , CM000664.1:g.179400900G>C	GRCh37
NC_000002.10:g.179109146G>C	NCBI36
NG_011618.3:g.299630C>G , LRG_391:g.299630C>G
NG_051363.1:g.18347G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.92870C>G (TTN)	ENSP00000343764.6:p.Pro30957Arg
ENST00000342175.11:c.73955C>G (TTN)	ENSP00000340554.6:p.Pro24652Arg
ENST00000359218.10:c.73754C>G (TTN)	ENSP00000352154.5:p.Pro24585Arg
ENST00000342175.10:c.73955C>G (TTN)	ENSP00000340554.6:p.Pro24652Arg
ENST00000342992.10:c.92870C>G (TTN)	ENSP00000343764.6:p.Pro30957Arg
ENST00000359218.9:c.73754C>G (TTN)	ENSP00000352154.5:p.Pro24585Arg
ENST00000460472.6:c.73379C>G (TTN)	ENSP00000434586.1:p.Pro24460Arg
ENST00000589042.5:c.100574C>G (TTN) MANE Select	ENSP00000467141.1:p.Pro33525Arg
ENST00000591111.5:c.95651C>G (TTN)	ENSP00000465570.1:p.Pro31884Arg
ENST00000615779.4:c.95651C>G (TTN)	ENSP00000483597.1:p.Pro31884Arg
NM_001256850.1:c.95651C>G (TTN)	NP_001243779.1:p.Pro31884Arg
NM_001267550.2:c.100574C>G (TTN) MANE Select	NP_001254479.2:p.Pro33525Arg
NM_003319.4:c.73379C>G (TTN)	NP_003310.4:p.Pro24460Arg
NM_133378.4:c.92870C>G (TTN)	NP_596869.4:p.Pro30957Arg
NM_133432.3:c.73754C>G (TTN)	NP_597676.3:p.Pro24585Arg
NM_133437.4:c.73955C>G (TTN)	NP_597681.4:p.Pro24652Arg
NR_038271.1:n.446+12537G>C (TTN-AS1)
NR_038272.1:n.316+345G>C (TTN-AS1)
XM_011511729.1:c.99671C>G (TTN)	XP_011510031.1:p.Pro33224Arg
XM_011511730.1:c.73565C>G (TTN)	XP_011510032.1:p.Pro24522Arg
XM_011511731.1:c.73424C>G (TTN)	XP_011510033.1:p.Pro24475Arg
XM_017004819.1:c.99467C>G (TTN)	XP_016860308.1:p.Pro33156Arg
XM_017004820.1:c.94865C>G (TTN)	XP_016860309.1:p.Pro31622Arg
XM_017004821.1:c.94862C>G (TTN)	XP_016860310.1:p.Pro31621Arg
XM_017004822.1:c.91904C>G (TTN)	XP_016860311.1:p.Pro30635Arg
XM_017004823.1:c.73520C>G (TTN)	XP_016860312.1:p.Pro24507Arg
XM_024453094.1:c.95015C>G (TTN)	XP_024308862.1:p.Pro31672Arg
XM_024453095.1:c.95012C>G (TTN)	XP_024308863.1:p.Pro31671Arg
XM_024453096.1:c.94445C>G (TTN)	XP_024308864.1:p.Pro31482Arg
XM_024453097.1:c.91787C>G (TTN)	XP_024308865.1:p.Pro30596Arg
XM_024453098.1:c.91706C>G (TTN)	XP_024308866.1:p.Pro30569Arg
XM_024453099.1:c.73469C>G (TTN)	XP_024308867.1:p.Pro24490Arg
XM_024453100.1:c.63323C>G (TTN)	XP_024308868.1:p.Pro21108Arg