Canonical Allele Identifier: CA349471608

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179411501C>A (hg19) ; chr2:g.178546774C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178546774C>A , CM000664.2:g.178546774C>A	GRCh38
NC_000002.11:g.179411501C>A , CM000664.1:g.179411501C>A	GRCh37
NC_000002.10:g.179119747C>A	NCBI36
NG_011618.3:g.289029G>T , LRG_391:g.289029G>T
NG_051363.1:g.28948C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.86950G>T (TTN)	ENSP00000343764.6:p.Gly28984Ter
ENST00000342175.11:c.68035G>T (TTN)	ENSP00000340554.6:p.Gly22679Ter
ENST00000359218.10:c.67834G>T (TTN)	ENSP00000352154.5:p.Gly22612Ter
ENST00000342175.10:c.68035G>T (TTN)	ENSP00000340554.6:p.Gly22679Ter
ENST00000342992.10:c.86950G>T (TTN)	ENSP00000343764.6:p.Gly28984Ter
ENST00000359218.9:c.67834G>T (TTN)	ENSP00000352154.5:p.Gly22612Ter
ENST00000460472.6:c.67459G>T (TTN)	ENSP00000434586.1:p.Gly22487Ter
ENST00000589042.5:c.94654G>T (TTN) MANE Select	ENSP00000467141.1:p.Gly31552Ter
ENST00000591111.5:c.89731G>T (TTN)	ENSP00000465570.1:p.Gly29911Ter
ENST00000615779.4:c.89731G>T (TTN)	ENSP00000483597.1:p.Gly29911Ter
NM_001256850.1:c.89731G>T (TTN)	NP_001243779.1:p.Gly29911Ter
NM_001267550.2:c.94654G>T (TTN) MANE Select	NP_001254479.2:p.Gly31552Ter
NM_003319.4:c.67459G>T (TTN)	NP_003310.4:p.Gly22487Ter
NM_133378.4:c.86950G>T (TTN)	NP_596869.4:p.Gly28984Ter
NM_133432.3:c.67834G>T (TTN)	NP_597676.3:p.Gly22612Ter
NM_133437.4:c.68035G>T (TTN)	NP_597681.4:p.Gly22679Ter
NR_038271.1:n.446+23138C>A (TTN-AS1)
NR_038272.1:n.2043+4413C>A (TTN-AS1)
XM_011511729.1:c.93751G>T (TTN)	XP_011510031.1:p.Gly31251Ter
XM_011511730.1:c.67645G>T (TTN)	XP_011510032.1:p.Gly22549Ter
XM_011511731.1:c.67504G>T (TTN)	XP_011510033.1:p.Gly22502Ter
XM_017004819.1:c.93547G>T (TTN)	XP_016860308.1:p.Gly31183Ter
XM_017004820.1:c.88945G>T (TTN)	XP_016860309.1:p.Gly29649Ter
XM_017004821.1:c.88942G>T (TTN)	XP_016860310.1:p.Gly29648Ter
XM_017004822.1:c.85984G>T (TTN)	XP_016860311.1:p.Gly28662Ter
XM_017004823.1:c.67600G>T (TTN)	XP_016860312.1:p.Gly22534Ter
XM_024453094.1:c.89095G>T (TTN)	XP_024308862.1:p.Gly29699Ter
XM_024453095.1:c.89092G>T (TTN)	XP_024308863.1:p.Gly29698Ter
XM_024453096.1:c.88525G>T (TTN)	XP_024308864.1:p.Gly29509Ter
XM_024453097.1:c.85867G>T (TTN)	XP_024308865.1:p.Gly28623Ter
XM_024453098.1:c.85786G>T (TTN)	XP_024308866.1:p.Gly28596Ter
XM_024453099.1:c.67549G>T (TTN)	XP_024308867.1:p.Gly22517Ter
XM_024453100.1:c.57403G>T (TTN)	XP_024308868.1:p.Gly19135Ter