Canonical Allele Identifier: CA349450949

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408622G>C (hg19) ; chr2:g.178543895G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543895G>C , CM000664.2:g.178543895G>C	GRCh38
NC_000002.11:g.179408622G>C , CM000664.1:g.179408622G>C	GRCh37
NC_000002.10:g.179116868G>C	NCBI36
NG_011618.3:g.291908C>G , LRG_391:g.291908C>G
NG_051363.1:g.26069G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88545C>G (TTN)	ENSP00000343764.6:p.Tyr29515Ter
ENST00000342175.11:c.69630C>G (TTN)	ENSP00000340554.6:p.Tyr23210Ter
ENST00000359218.10:c.69429C>G (TTN)	ENSP00000352154.5:p.Tyr23143Ter
ENST00000342175.10:c.69630C>G (TTN)	ENSP00000340554.6:p.Tyr23210Ter
ENST00000342992.10:c.88545C>G (TTN)	ENSP00000343764.6:p.Tyr29515Ter
ENST00000359218.9:c.69429C>G (TTN)	ENSP00000352154.5:p.Tyr23143Ter
ENST00000460472.6:c.69054C>G (TTN)	ENSP00000434586.1:p.Tyr23018Ter
ENST00000589042.5:c.96249C>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr32083Ter
ENST00000591111.5:c.91326C>G (TTN)	ENSP00000465570.1:p.Tyr30442Ter
ENST00000615779.4:c.91326C>G (TTN)	ENSP00000483597.1:p.Tyr30442Ter
NM_001256850.1:c.91326C>G (TTN)	NP_001243779.1:p.Tyr30442Ter
NM_001267550.2:c.96249C>G (TTN) MANE Select	NP_001254479.2:p.Tyr32083Ter
NM_003319.4:c.69054C>G (TTN)	NP_003310.4:p.Tyr23018Ter
NM_133378.4:c.88545C>G (TTN)	NP_596869.4:p.Tyr29515Ter
NM_133432.3:c.69429C>G (TTN)	NP_597676.3:p.Tyr23143Ter
NM_133437.4:c.69630C>G (TTN)	NP_597681.4:p.Tyr23210Ter
NR_038271.1:n.446+20259G>C (TTN-AS1)
NR_038272.1:n.2043+1534G>C (TTN-AS1)
XM_011511729.1:c.95346C>G (TTN)	XP_011510031.1:p.Tyr31782Ter
XM_011511730.1:c.69240C>G (TTN)	XP_011510032.1:p.Tyr23080Ter
XM_011511731.1:c.69099C>G (TTN)	XP_011510033.1:p.Tyr23033Ter
XM_017004819.1:c.95142C>G (TTN)	XP_016860308.1:p.Tyr31714Ter
XM_017004820.1:c.90540C>G (TTN)	XP_016860309.1:p.Tyr30180Ter
XM_017004821.1:c.90537C>G (TTN)	XP_016860310.1:p.Tyr30179Ter
XM_017004822.1:c.87579C>G (TTN)	XP_016860311.1:p.Tyr29193Ter
XM_017004823.1:c.69195C>G (TTN)	XP_016860312.1:p.Tyr23065Ter
XM_024453094.1:c.90690C>G (TTN)	XP_024308862.1:p.Tyr30230Ter
XM_024453095.1:c.90687C>G (TTN)	XP_024308863.1:p.Tyr30229Ter
XM_024453096.1:c.90120C>G (TTN)	XP_024308864.1:p.Tyr30040Ter
XM_024453097.1:c.87462C>G (TTN)	XP_024308865.1:p.Tyr29154Ter
XM_024453098.1:c.87381C>G (TTN)	XP_024308866.1:p.Tyr29127Ter
XM_024453099.1:c.69144C>G (TTN)	XP_024308867.1:p.Tyr23048Ter
XM_024453100.1:c.58998C>G (TTN)	XP_024308868.1:p.Tyr19666Ter