Canonical Allele Identifier: CA349525329

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178598777G>C , CM000664.2:g.178598777G>C	GRCh38
NC_000002.11:g.179463504G>C , CM000664.1:g.179463504G>C	GRCh37
NC_000002.10:g.179171749G>C	NCBI36
NG_011618.3:g.237026C>G , LRG_391:g.237026C>G
NG_051363.1:g.80951G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.56933C>G (TTN) MANE Select	NP_001254479.2:p.Ser18978Ter
ENST00000589042.5:c.56933C>G (TTN) MANE Select	ENSP00000467141.1:p.Ser18978Ter
NM_001256850.1:c.52010C>G (TTN)	NP_001243779.1:p.Ser17337Ter
NM_003319.4:c.29738C>G (TTN)	NP_003310.4:p.Ser9913Ter
NM_133378.4:c.49229C>G (TTN)	NP_596869.4:p.Ser16410Ter
NM_133432.3:c.30113C>G (TTN)	NP_597676.3:p.Ser10038Ter
NM_133437.4:c.30314C>G (TTN)	NP_597681.4:p.Ser10105Ter
NR_038271.1:n.682+1096G>C (TTN-AS1)
NR_038272.1:n.3568+104G>C (TTN-AS1)
ENST00000342175.10:c.30314C>G (TTN)	ENSP00000340554.6:p.Ser10105Ter
ENST00000342175.11:c.30314C>G (TTN)	ENSP00000340554.6:p.Ser10105Ter
ENST00000342992.10:c.49229C>G (TTN)	ENSP00000343764.6:p.Ser16410Ter
ENST00000342992.11:c.49229C>G (TTN)	ENSP00000343764.6:p.Ser16410Ter
ENST00000359218.10:c.30113C>G (TTN)	ENSP00000352154.5:p.Ser10038Ter
ENST00000359218.9:c.30113C>G (TTN)	ENSP00000352154.5:p.Ser10038Ter
ENST00000460472.6:c.29738C>G (TTN)	ENSP00000434586.1:p.Ser9913Ter
ENST00000591111.5:c.52010C>G (TTN)	ENSP00000465570.1:p.Ser17337Ter
ENST00000615779.4:c.52010C>G (TTN)	ENSP00000483597.1:p.Ser17337Ter
XM_011511729.1:c.56030C>G (TTN)	XP_011510031.1:p.Ser18677Ter
XM_011511730.1:c.29924C>G (TTN)	XP_011510032.1:p.Ser9975Ter
XM_011511731.1:c.29783C>G (TTN)	XP_011510033.1:p.Ser9928Ter
XM_017004819.1:c.55826C>G (TTN)	XP_016860308.1:p.Ser18609Ter
XM_017004820.1:c.51224C>G (TTN)	XP_016860309.1:p.Ser17075Ter
XM_017004821.1:c.51221C>G (TTN)	XP_016860310.1:p.Ser17074Ter
XM_017004822.1:c.48263C>G (TTN)	XP_016860311.1:p.Ser16088Ter
XM_017004823.1:c.29879C>G (TTN)	XP_016860312.1:p.Ser9960Ter
XM_024453094.1:c.51374C>G (TTN)	XP_024308862.1:p.Ser17125Ter
XM_024453095.1:c.51371C>G (TTN)	XP_024308863.1:p.Ser17124Ter
XM_024453096.1:c.50804C>G (TTN)	XP_024308864.1:p.Ser16935Ter
XM_024453097.1:c.48146C>G (TTN)	XP_024308865.1:p.Ser16049Ter
XM_024453098.1:c.48065C>G (TTN)	XP_024308866.1:p.Ser16022Ter
XM_024453099.1:c.29828C>G (TTN)	XP_024308867.1:p.Ser9943Ter
XM_024453100.1:c.19682C>G (TTN)	XP_024308868.1:p.Ser6561Ter