Canonical Allele Identifier: CA349652133

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179497707A>G (hg19) ; chr2:g.178632980A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178632980A>G , CM000664.2:g.178632980A>G	GRCh38
NC_000002.11:g.179497707A>G , CM000664.1:g.179497707A>G	GRCh37
NC_000002.10:g.179205952A>G	NCBI36
NG_011618.3:g.202823T>C , LRG_391:g.202823T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.35447T>C	ENSP00000343764.6:p.Met11816Thr
ENST00000342175.11:c.16532T>C	ENSP00000340554.6:p.Met5511Thr
ENST00000359218.10:c.16331T>C	ENSP00000352154.5:p.Met5444Thr
ENST00000342175.10:c.16532T>C	ENSP00000340554.6:p.Met5511Thr
ENST00000342992.10:c.35447T>C	ENSP00000343764.6:p.Met11816Thr
ENST00000359218.9:c.16331T>C	ENSP00000352154.5:p.Met5444Thr
ENST00000460472.6:c.15956T>C	ENSP00000434586.1:p.Met5319Thr
ENST00000589042.5:c.43151T>C MANE Select	ENSP00000467141.1:p.Met14384Thr
ENST00000591111.5:c.38228T>C	ENSP00000465570.1:p.Met12743Thr
ENST00000615779.4:c.38228T>C	ENSP00000483597.1:p.Met12743Thr
NM_001256850.1:c.38228T>C	NP_001243779.1:p.Met12743Thr
NM_001267550.2:c.43151T>C MANE Select	NP_001254479.2:p.Met14384Thr
NM_003319.4:c.15956T>C	NP_003310.4:p.Met5319Thr
NM_133378.4:c.35447T>C	NP_596869.4:p.Met11816Thr
NM_133432.3:c.16331T>C	NP_597676.3:p.Met5444Thr
NM_133437.4:c.16532T>C	NP_597681.4:p.Met5511Thr
XM_011511729.1:c.42248T>C	XP_011510031.1:p.Met14083Thr
XM_011511730.1:c.16142T>C	XP_011510032.1:p.Met5381Thr
XM_011511731.1:c.16001T>C	XP_011510033.1:p.Met5334Thr
XM_017004819.1:c.42044T>C	XP_016860308.1:p.Met14015Thr
XM_017004820.1:c.37442T>C	XP_016860309.1:p.Met12481Thr
XM_017004821.1:c.37439T>C	XP_016860310.1:p.Met12480Thr
XM_017004822.1:c.34481T>C	XP_016860311.1:p.Met11494Thr
XM_017004823.1:c.16097T>C	XP_016860312.1:p.Met5366Thr
XM_024453094.1:c.37592T>C	XP_024308862.1:p.Met12531Thr
XM_024453095.1:c.37589T>C	XP_024308863.1:p.Met12530Thr
XM_024453096.1:c.37022T>C	XP_024308864.1:p.Met12341Thr
XM_024453097.1:c.34364T>C	XP_024308865.1:p.Met11455Thr
XM_024453098.1:c.34283T>C	XP_024308866.1:p.Met11428Thr
XM_024453099.1:c.16046T>C	XP_024308867.1:p.Met5349Thr
XM_024453100.1:c.5900T>C	XP_024308868.1:p.Met1967Thr