Canonical Allele Identifier: CA349427833

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179402319T>G (hg19) ; chr2:g.178537592T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178537592T>G , CM000664.2:g.178537592T>G	GRCh38
NC_000002.11:g.179402319T>G , CM000664.1:g.179402319T>G	GRCh37
NC_000002.10:g.179110565T>G	NCBI36
NG_011618.3:g.298211A>C , LRG_391:g.298211A>C
NG_051363.1:g.19766T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.91911A>C (TTN)	ENSP00000343764.6:p.Lys30637Asn
ENST00000342175.11:c.72996A>C (TTN)	ENSP00000340554.6:p.Lys24332Asn
ENST00000359218.10:c.72795A>C (TTN)	ENSP00000352154.5:p.Lys24265Asn
ENST00000342175.10:c.72996A>C (TTN)	ENSP00000340554.6:p.Lys24332Asn
ENST00000342992.10:c.91911A>C (TTN)	ENSP00000343764.6:p.Lys30637Asn
ENST00000359218.9:c.72795A>C (TTN)	ENSP00000352154.5:p.Lys24265Asn
ENST00000460472.6:c.72420A>C (TTN)	ENSP00000434586.1:p.Lys24140Asn
ENST00000589042.5:c.99615A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys33205Asn
ENST00000591111.5:c.94692A>C (TTN)	ENSP00000465570.1:p.Lys31564Asn
ENST00000615779.4:c.94692A>C (TTN)	ENSP00000483597.1:p.Lys31564Asn
NM_001256850.1:c.94692A>C (TTN)	NP_001243779.1:p.Lys31564Asn
NM_001267550.2:c.99615A>C (TTN) MANE Select	NP_001254479.2:p.Lys33205Asn
NM_003319.4:c.72420A>C (TTN)	NP_003310.4:p.Lys24140Asn
NM_133378.4:c.91911A>C (TTN)	NP_596869.4:p.Lys30637Asn
NM_133432.3:c.72795A>C (TTN)	NP_597676.3:p.Lys24265Asn
NM_133437.4:c.72996A>C (TTN)	NP_597681.4:p.Lys24332Asn
NR_038271.1:n.446+13956T>G (TTN-AS1)
NR_038272.1:n.548T>G (TTN-AS1)
XM_011511729.1:c.98712A>C (TTN)	XP_011510031.1:p.Lys32904Asn
XM_011511730.1:c.72606A>C (TTN)	XP_011510032.1:p.Lys24202Asn
XM_011511731.1:c.72465A>C (TTN)	XP_011510033.1:p.Lys24155Asn
XM_017004819.1:c.98508A>C (TTN)	XP_016860308.1:p.Lys32836Asn
XM_017004820.1:c.93906A>C (TTN)	XP_016860309.1:p.Lys31302Asn
XM_017004821.1:c.93903A>C (TTN)	XP_016860310.1:p.Lys31301Asn
XM_017004822.1:c.90945A>C (TTN)	XP_016860311.1:p.Lys30315Asn
XM_017004823.1:c.72561A>C (TTN)	XP_016860312.1:p.Lys24187Asn
XM_024453094.1:c.94056A>C (TTN)	XP_024308862.1:p.Lys31352Asn
XM_024453095.1:c.94053A>C (TTN)	XP_024308863.1:p.Lys31351Asn
XM_024453096.1:c.93486A>C (TTN)	XP_024308864.1:p.Lys31162Asn
XM_024453097.1:c.90828A>C (TTN)	XP_024308865.1:p.Lys30276Asn
XM_024453098.1:c.90747A>C (TTN)	XP_024308866.1:p.Lys30249Asn
XM_024453099.1:c.72510A>C (TTN)	XP_024308867.1:p.Lys24170Asn
XM_024453100.1:c.62364A>C (TTN)	XP_024308868.1:p.Lys20788Asn