Canonical Allele Identifier: CA430239348

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179402301A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178537574A>C , CM000664.2:g.178537574A>C	GRCh38
NC_000002.11:g.179402301A>C , CM000664.1:g.179402301A>C	GRCh37
NC_000002.10:g.179110547A>C	NCBI36
NG_011618.3:g.298229T>G , LRG_391:g.298229T>G
NG_051363.1:g.19748A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.91929T>G (TTN)	ENSP00000343764.6:p.Gly30643=
ENST00000342175.11:c.73014T>G (TTN)	ENSP00000340554.6:p.Gly24338=
ENST00000359218.10:c.72813T>G (TTN)	ENSP00000352154.5:p.Gly24271=
ENST00000342175.10:c.73014T>G (TTN)	ENSP00000340554.6:p.Gly24338=
ENST00000342992.10:c.91929T>G (TTN)	ENSP00000343764.6:p.Gly30643=
ENST00000359218.9:c.72813T>G (TTN)	ENSP00000352154.5:p.Gly24271=
ENST00000460472.6:c.72438T>G (TTN)	ENSP00000434586.1:p.Gly24146=
ENST00000589042.5:c.99633T>G (TTN) MANE Select	ENSP00000467141.1:p.Gly33211=
ENST00000591111.5:c.94710T>G (TTN)	ENSP00000465570.1:p.Gly31570=
ENST00000615779.4:c.94710T>G (TTN)	ENSP00000483597.1:p.Gly31570=
NM_001256850.1:c.94710T>G (TTN)	NP_001243779.1:p.Gly31570=
NM_001267550.2:c.99633T>G (TTN) MANE Select	NP_001254479.2:p.Gly33211=
NM_003319.4:c.72438T>G (TTN)	NP_003310.4:p.Gly24146=
NM_133378.4:c.91929T>G (TTN)	NP_596869.4:p.Gly30643=
NM_133432.3:c.72813T>G (TTN)	NP_597676.3:p.Gly24271=
NM_133437.4:c.73014T>G (TTN)	NP_597681.4:p.Gly24338=
NR_038271.1:n.446+13938A>C (TTN-AS1)
NR_038272.1:n.530A>C (TTN-AS1)
XM_011511729.1:c.98730T>G (TTN)	XP_011510031.1:p.Gly32910=
XM_011511730.1:c.72624T>G (TTN)	XP_011510032.1:p.Gly24208=
XM_011511731.1:c.72483T>G (TTN)	XP_011510033.1:p.Gly24161=
XM_017004819.1:c.98526T>G (TTN)	XP_016860308.1:p.Gly32842=
XM_017004820.1:c.93924T>G (TTN)	XP_016860309.1:p.Gly31308=
XM_017004821.1:c.93921T>G (TTN)	XP_016860310.1:p.Gly31307=
XM_017004822.1:c.90963T>G (TTN)	XP_016860311.1:p.Gly30321=
XM_017004823.1:c.72579T>G (TTN)	XP_016860312.1:p.Gly24193=
XM_024453094.1:c.94074T>G (TTN)	XP_024308862.1:p.Gly31358=
XM_024453095.1:c.94071T>G (TTN)	XP_024308863.1:p.Gly31357=
XM_024453096.1:c.93504T>G (TTN)	XP_024308864.1:p.Gly31168=
XM_024453097.1:c.90846T>G (TTN)	XP_024308865.1:p.Gly30282=
XM_024453098.1:c.90765T>G (TTN)	XP_024308866.1:p.Gly30255=
XM_024453099.1:c.72528T>G (TTN)	XP_024308867.1:p.Gly24176=
XM_024453100.1:c.62382T>G (TTN)	XP_024308868.1:p.Gly20794=