Canonical Allele Identifier: CA349429871

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179447078T>G (hg19) ; chr2:g.178582351T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178582351T>G , CM000664.2:g.178582351T>G	GRCh38
NC_000002.11:g.179447078T>G , CM000664.1:g.179447078T>G	GRCh37
NC_000002.10:g.179155324T>G	NCBI36
NG_011618.3:g.253452A>C , LRG_391:g.253452A>C
NG_051363.1:g.64525T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.58401A>C (TTN)	ENSP00000343764.6:p.Lys19467Asn
ENST00000342175.11:c.39486A>C (TTN)	ENSP00000340554.6:p.Lys13162Asn
ENST00000359218.10:c.39285A>C (TTN)	ENSP00000352154.5:p.Lys13095Asn
ENST00000342175.10:c.39486A>C (TTN)	ENSP00000340554.6:p.Lys13162Asn
ENST00000342992.10:c.58401A>C (TTN)	ENSP00000343764.6:p.Lys19467Asn
ENST00000359218.9:c.39285A>C (TTN)	ENSP00000352154.5:p.Lys13095Asn
ENST00000460472.6:c.38910A>C (TTN)	ENSP00000434586.1:p.Lys12970Asn
ENST00000589042.5:c.66105A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys22035Asn
ENST00000591111.5:c.61182A>C (TTN)	ENSP00000465570.1:p.Lys20394Asn
ENST00000615779.4:c.61182A>C (TTN)	ENSP00000483597.1:p.Lys20394Asn
NM_001256850.1:c.61182A>C (TTN)	NP_001243779.1:p.Lys20394Asn
NM_001267550.2:c.66105A>C (TTN) MANE Select	NP_001254479.2:p.Lys22035Asn
NM_003319.4:c.38910A>C (TTN)	NP_003310.4:p.Lys12970Asn
NM_133378.4:c.58401A>C (TTN)	NP_596869.4:p.Lys19467Asn
NM_133432.3:c.39285A>C (TTN)	NP_597676.3:p.Lys13095Asn
NM_133437.4:c.39486A>C (TTN)	NP_597681.4:p.Lys13162Asn
NR_038271.1:n.596+10902T>G (TTN-AS1)
NR_038272.1:n.2044-221T>G (TTN-AS1)
XM_011511729.1:c.65202A>C (TTN)	XP_011510031.1:p.Lys21734Asn
XM_011511730.1:c.39096A>C (TTN)	XP_011510032.1:p.Lys13032Asn
XM_011511731.1:c.38955A>C (TTN)	XP_011510033.1:p.Lys12985Asn
XM_017004819.1:c.64998A>C (TTN)	XP_016860308.1:p.Lys21666Asn
XM_017004820.1:c.60396A>C (TTN)	XP_016860309.1:p.Lys20132Asn
XM_017004821.1:c.60393A>C (TTN)	XP_016860310.1:p.Lys20131Asn
XM_017004822.1:c.57435A>C (TTN)	XP_016860311.1:p.Lys19145Asn
XM_017004823.1:c.39051A>C (TTN)	XP_016860312.1:p.Lys13017Asn
XM_024453094.1:c.60546A>C (TTN)	XP_024308862.1:p.Lys20182Asn
XM_024453095.1:c.60543A>C (TTN)	XP_024308863.1:p.Lys20181Asn
XM_024453096.1:c.59976A>C (TTN)	XP_024308864.1:p.Lys19992Asn
XM_024453097.1:c.57318A>C (TTN)	XP_024308865.1:p.Lys19106Asn
XM_024453098.1:c.57237A>C (TTN)	XP_024308866.1:p.Lys19079Asn
XM_024453099.1:c.39000A>C (TTN)	XP_024308867.1:p.Lys13000Asn
XM_024453100.1:c.28854A>C (TTN)	XP_024308868.1:p.Lys9618Asn