Canonical Allele Identifier: CA349608025

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614738A>C , CM000664.2:g.178614738A>C	GRCh38
NC_000002.11:g.179479465A>C , CM000664.1:g.179479465A>C	GRCh37
NC_000002.10:g.179187710A>C	NCBI36
NG_011618.3:g.221065T>G , LRG_391:g.221065T>G
NG_051363.1:g.96912A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.48776T>G (TTN) MANE Select	NP_001254479.2:p.Phe16259Cys
ENST00000589042.5:c.48776T>G (TTN) MANE Select	ENSP00000467141.1:p.Phe16259Cys
NM_001256850.1:c.43853T>G (TTN)	NP_001243779.1:p.Phe14618Cys
NM_003319.4:c.21581T>G (TTN)	NP_003310.4:p.Phe7194Cys
NM_133378.4:c.41072T>G (TTN)	NP_596869.4:p.Phe13691Cys
NM_133432.3:c.21956T>G (TTN)	NP_597676.3:p.Phe7319Cys
NM_133437.4:c.22157T>G (TTN)	NP_597681.4:p.Phe7386Cys
NR_038271.1:n.1486A>C (TTN-AS1)
ENST00000342175.10:c.22157T>G (TTN)	ENSP00000340554.6:p.Phe7386Cys
ENST00000342175.11:c.22157T>G (TTN)	ENSP00000340554.6:p.Phe7386Cys
ENST00000342992.10:c.41072T>G (TTN)	ENSP00000343764.6:p.Phe13691Cys
ENST00000342992.11:c.41072T>G (TTN)	ENSP00000343764.6:p.Phe13691Cys
ENST00000359218.10:c.21956T>G (TTN)	ENSP00000352154.5:p.Phe7319Cys
ENST00000359218.9:c.21956T>G (TTN)	ENSP00000352154.5:p.Phe7319Cys
ENST00000460472.6:c.21581T>G (TTN)	ENSP00000434586.1:p.Phe7194Cys
ENST00000591111.5:c.43853T>G (TTN)	ENSP00000465570.1:p.Phe14618Cys
ENST00000615779.4:c.43853T>G (TTN)	ENSP00000483597.1:p.Phe14618Cys
XM_011511729.1:c.47873T>G (TTN)	XP_011510031.1:p.Phe15958Cys
XM_011511730.1:c.21767T>G (TTN)	XP_011510032.1:p.Phe7256Cys
XM_011511731.1:c.21626T>G (TTN)	XP_011510033.1:p.Phe7209Cys
XM_017004819.1:c.47669T>G (TTN)	XP_016860308.1:p.Phe15890Cys
XM_017004820.1:c.43067T>G (TTN)	XP_016860309.1:p.Phe14356Cys
XM_017004821.1:c.43064T>G (TTN)	XP_016860310.1:p.Phe14355Cys
XM_017004822.1:c.40106T>G (TTN)	XP_016860311.1:p.Phe13369Cys
XM_017004823.1:c.21722T>G (TTN)	XP_016860312.1:p.Phe7241Cys
XM_024453094.1:c.43217T>G (TTN)	XP_024308862.1:p.Phe14406Cys
XM_024453095.1:c.43214T>G (TTN)	XP_024308863.1:p.Phe14405Cys
XM_024453096.1:c.42647T>G (TTN)	XP_024308864.1:p.Phe14216Cys
XM_024453097.1:c.39989T>G (TTN)	XP_024308865.1:p.Phe13330Cys
XM_024453098.1:c.39908T>G (TTN)	XP_024308866.1:p.Phe13303Cys
XM_024453099.1:c.21671T>G (TTN)	XP_024308867.1:p.Phe7224Cys
XM_024453100.1:c.11525T>G (TTN)	XP_024308868.1:p.Phe3842Cys