Canonical Allele Identifier: CA349582284

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178564878G>C , CM000664.2:g.178564878G>C	GRCh38
NC_000002.11:g.179429605G>C , CM000664.1:g.179429605G>C	GRCh37
NC_000002.10:g.179137851G>C	NCBI36
NG_011618.3:g.270925C>G , LRG_391:g.270925C>G
NG_051363.1:g.47052G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.81254C>G (TTN) MANE Select	NP_001254479.2:p.Ser27085Ter
ENST00000589042.5:c.81254C>G (TTN) MANE Select	ENSP00000467141.1:p.Ser27085Ter
NM_001256850.1:c.76331C>G (TTN)	NP_001243779.1:p.Ser25444Ter
NM_003319.4:c.54059C>G (TTN)	NP_003310.4:p.Ser18020Ter
NM_133378.4:c.73550C>G (TTN)	NP_596869.4:p.Ser24517Ter
NM_133432.3:c.54434C>G (TTN)	NP_597676.3:p.Ser18145Ter
NM_133437.4:c.54635C>G (TTN)	NP_597681.4:p.Ser18212Ter
NR_038271.1:n.447-6422G>C (TTN-AS1)
NR_038272.1:n.2044-17694G>C (TTN-AS1)
ENST00000342175.10:c.54635C>G (TTN)	ENSP00000340554.6:p.Ser18212Ter
ENST00000342175.11:c.54635C>G (TTN)	ENSP00000340554.6:p.Ser18212Ter
ENST00000342992.10:c.73550C>G (TTN)	ENSP00000343764.6:p.Ser24517Ter
ENST00000342992.11:c.73550C>G (TTN)	ENSP00000343764.6:p.Ser24517Ter
ENST00000359218.10:c.54434C>G (TTN)	ENSP00000352154.5:p.Ser18145Ter
ENST00000359218.9:c.54434C>G (TTN)	ENSP00000352154.5:p.Ser18145Ter
ENST00000460472.6:c.54059C>G (TTN)	ENSP00000434586.1:p.Ser18020Ter
ENST00000591111.5:c.76331C>G (TTN)	ENSP00000465570.1:p.Ser25444Ter
ENST00000615779.4:c.76331C>G (TTN)	ENSP00000483597.1:p.Ser25444Ter
XM_011511729.1:c.80351C>G (TTN)	XP_011510031.1:p.Ser26784Ter
XM_011511730.1:c.54245C>G (TTN)	XP_011510032.1:p.Ser18082Ter
XM_011511731.1:c.54104C>G (TTN)	XP_011510033.1:p.Ser18035Ter
XM_017004819.1:c.80147C>G (TTN)	XP_016860308.1:p.Ser26716Ter
XM_017004820.1:c.75545C>G (TTN)	XP_016860309.1:p.Ser25182Ter
XM_017004821.1:c.75542C>G (TTN)	XP_016860310.1:p.Ser25181Ter
XM_017004822.1:c.72584C>G (TTN)	XP_016860311.1:p.Ser24195Ter
XM_017004823.1:c.54200C>G (TTN)	XP_016860312.1:p.Ser18067Ter
XM_024453094.1:c.75695C>G (TTN)	XP_024308862.1:p.Ser25232Ter
XM_024453095.1:c.75692C>G (TTN)	XP_024308863.1:p.Ser25231Ter
XM_024453096.1:c.75125C>G (TTN)	XP_024308864.1:p.Ser25042Ter
XM_024453097.1:c.72467C>G (TTN)	XP_024308865.1:p.Ser24156Ter
XM_024453098.1:c.72386C>G (TTN)	XP_024308866.1:p.Ser24129Ter
XM_024453099.1:c.54149C>G (TTN)	XP_024308867.1:p.Ser18050Ter
XM_024453100.1:c.44003C>G (TTN)	XP_024308868.1:p.Ser14668Ter