Canonical Allele Identifier: CA349411751

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396913G>C (hg19) ; chr2:g.178532186G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532186G>C , CM000664.2:g.178532186G>C	GRCh38
NC_000002.11:g.179396913G>C , CM000664.1:g.179396913G>C	GRCh37
NC_000002.10:g.179105159G>C	NCBI36
NG_011618.3:g.303617C>G , LRG_391:g.303617C>G
NG_051363.1:g.14360G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96725C>G (TTN)	ENSP00000343764.6:p.Thr32242Arg
ENST00000342175.11:c.77810C>G (TTN)	ENSP00000340554.6:p.Thr25937Arg
ENST00000359218.10:c.77609C>G (TTN)	ENSP00000352154.5:p.Thr25870Arg
ENST00000342175.10:c.77810C>G (TTN)	ENSP00000340554.6:p.Thr25937Arg
ENST00000342992.10:c.96725C>G (TTN)	ENSP00000343764.6:p.Thr32242Arg
ENST00000359218.9:c.77609C>G (TTN)	ENSP00000352154.5:p.Thr25870Arg
ENST00000460472.6:c.77234C>G (TTN)	ENSP00000434586.1:p.Thr25745Arg
ENST00000589042.5:c.104429C>G (TTN) MANE Select	ENSP00000467141.1:p.Thr34810Arg
ENST00000591111.5:c.99506C>G (TTN)	ENSP00000465570.1:p.Thr33169Arg
ENST00000615779.4:c.99506C>G (TTN)	ENSP00000483597.1:p.Thr33169Arg
NM_001256850.1:c.99506C>G (TTN)	NP_001243779.1:p.Thr33169Arg
NM_001267550.2:c.104429C>G (TTN) MANE Select	NP_001254479.2:p.Thr34810Arg
NM_003319.4:c.77234C>G (TTN)	NP_003310.4:p.Thr25745Arg
NM_133378.4:c.96725C>G (TTN)	NP_596869.4:p.Thr32242Arg
NM_133432.3:c.77609C>G (TTN)	NP_597676.3:p.Thr25870Arg
NM_133437.4:c.77810C>G (TTN)	NP_597681.4:p.Thr25937Arg
NR_038271.1:n.446+8550G>C (TTN-AS1)
NR_038272.1:n.220-3546G>C (TTN-AS1)
XM_011511729.1:c.103526C>G (TTN)	XP_011510031.1:p.Thr34509Arg
XM_011511730.1:c.77420C>G (TTN)	XP_011510032.1:p.Thr25807Arg
XM_011511731.1:c.77279C>G (TTN)	XP_011510033.1:p.Thr25760Arg
XM_017004819.1:c.103322C>G (TTN)	XP_016860308.1:p.Thr34441Arg
XM_017004820.1:c.98720C>G (TTN)	XP_016860309.1:p.Thr32907Arg
XM_017004821.1:c.98717C>G (TTN)	XP_016860310.1:p.Thr32906Arg
XM_017004822.1:c.95759C>G (TTN)	XP_016860311.1:p.Thr31920Arg
XM_017004823.1:c.77375C>G (TTN)	XP_016860312.1:p.Thr25792Arg
XM_024453094.1:c.98870C>G (TTN)	XP_024308862.1:p.Thr32957Arg
XM_024453095.1:c.98867C>G (TTN)	XP_024308863.1:p.Thr32956Arg
XM_024453096.1:c.98300C>G (TTN)	XP_024308864.1:p.Thr32767Arg
XM_024453097.1:c.95642C>G (TTN)	XP_024308865.1:p.Thr31881Arg
XM_024453098.1:c.95561C>G (TTN)	XP_024308866.1:p.Thr31854Arg
XM_024453099.1:c.77324C>G (TTN)	XP_024308867.1:p.Thr25775Arg
XM_024453100.1:c.67178C>G (TTN)	XP_024308868.1:p.Thr22393Arg