Canonical Allele Identifier: CA349646335

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179495652A>C (hg19) ; chr2:g.178630925A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178630925A>C , CM000664.2:g.178630925A>C	GRCh38
NC_000002.11:g.179495652A>C , CM000664.1:g.179495652A>C	GRCh37
NC_000002.10:g.179203897A>C	NCBI36
NG_011618.3:g.204878T>G , LRG_391:g.204878T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.36329T>G	ENSP00000343764.6:p.Val12110Gly
ENST00000342175.11:c.17414T>G	ENSP00000340554.6:p.Val5805Gly
ENST00000359218.10:c.17213T>G	ENSP00000352154.5:p.Val5738Gly
ENST00000342175.10:c.17414T>G	ENSP00000340554.6:p.Val5805Gly
ENST00000342992.10:c.36329T>G	ENSP00000343764.6:p.Val12110Gly
ENST00000359218.9:c.17213T>G	ENSP00000352154.5:p.Val5738Gly
ENST00000460472.6:c.16838T>G	ENSP00000434586.1:p.Val5613Gly
ENST00000589042.5:c.44033T>G MANE Select	ENSP00000467141.1:p.Val14678Gly
ENST00000591111.5:c.39110T>G	ENSP00000465570.1:p.Val13037Gly
ENST00000615779.4:c.39110T>G	ENSP00000483597.1:p.Val13037Gly
NM_001256850.1:c.39110T>G	NP_001243779.1:p.Val13037Gly
NM_001267550.2:c.44033T>G MANE Select	NP_001254479.2:p.Val14678Gly
NM_003319.4:c.16838T>G	NP_003310.4:p.Val5613Gly
NM_133378.4:c.36329T>G	NP_596869.4:p.Val12110Gly
NM_133432.3:c.17213T>G	NP_597676.3:p.Val5738Gly
NM_133437.4:c.17414T>G	NP_597681.4:p.Val5805Gly
XM_011511729.1:c.43130T>G	XP_011510031.1:p.Val14377Gly
XM_011511730.1:c.17024T>G	XP_011510032.1:p.Val5675Gly
XM_011511731.1:c.16883T>G	XP_011510033.1:p.Val5628Gly
XM_017004819.1:c.42926T>G	XP_016860308.1:p.Val14309Gly
XM_017004820.1:c.38324T>G	XP_016860309.1:p.Val12775Gly
XM_017004821.1:c.38321T>G	XP_016860310.1:p.Val12774Gly
XM_017004822.1:c.35363T>G	XP_016860311.1:p.Val11788Gly
XM_017004823.1:c.16979T>G	XP_016860312.1:p.Val5660Gly
XM_024453094.1:c.38474T>G	XP_024308862.1:p.Val12825Gly
XM_024453095.1:c.38471T>G	XP_024308863.1:p.Val12824Gly
XM_024453096.1:c.37904T>G	XP_024308864.1:p.Val12635Gly
XM_024453097.1:c.35246T>G	XP_024308865.1:p.Val11749Gly
XM_024453098.1:c.35165T>G	XP_024308866.1:p.Val11722Gly
XM_024453099.1:c.16928T>G	XP_024308867.1:p.Val5643Gly
XM_024453100.1:c.6782T>G	XP_024308868.1:p.Val2261Gly