Canonical Allele Identifier: CA349607613

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178614637T>C , CM000664.2:g.178614637T>C	GRCh38
NC_000002.11:g.179479364T>C , CM000664.1:g.179479364T>C	GRCh37
NC_000002.10:g.179187609T>C	NCBI36
NG_011618.3:g.221166A>G , LRG_391:g.221166A>G
NG_051363.1:g.96811T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.48877A>G (TTN) MANE Select	NP_001254479.2:p.Thr16293Ala
ENST00000589042.5:c.48877A>G (TTN) MANE Select	ENSP00000467141.1:p.Thr16293Ala
NM_001256850.1:c.43954A>G (TTN)	NP_001243779.1:p.Thr14652Ala
NM_003319.4:c.21682A>G (TTN)	NP_003310.4:p.Thr7228Ala
NM_133378.4:c.41173A>G (TTN)	NP_596869.4:p.Thr13725Ala
NM_133432.3:c.22057A>G (TTN)	NP_597676.3:p.Thr7353Ala
NM_133437.4:c.22258A>G (TTN)	NP_597681.4:p.Thr7420Ala
NR_038271.1:n.1385T>C (TTN-AS1)
ENST00000342175.10:c.22258A>G (TTN)	ENSP00000340554.6:p.Thr7420Ala
ENST00000342175.11:c.22258A>G (TTN)	ENSP00000340554.6:p.Thr7420Ala
ENST00000342992.10:c.41173A>G (TTN)	ENSP00000343764.6:p.Thr13725Ala
ENST00000342992.11:c.41173A>G (TTN)	ENSP00000343764.6:p.Thr13725Ala
ENST00000359218.10:c.22057A>G (TTN)	ENSP00000352154.5:p.Thr7353Ala
ENST00000359218.9:c.22057A>G (TTN)	ENSP00000352154.5:p.Thr7353Ala
ENST00000460472.6:c.21682A>G (TTN)	ENSP00000434586.1:p.Thr7228Ala
ENST00000591111.5:c.43954A>G (TTN)	ENSP00000465570.1:p.Thr14652Ala
ENST00000615779.4:c.43954A>G (TTN)	ENSP00000483597.1:p.Thr14652Ala
XM_011511729.1:c.47974A>G (TTN)	XP_011510031.1:p.Thr15992Ala
XM_011511730.1:c.21868A>G (TTN)	XP_011510032.1:p.Thr7290Ala
XM_011511731.1:c.21727A>G (TTN)	XP_011510033.1:p.Thr7243Ala
XM_017004819.1:c.47770A>G (TTN)	XP_016860308.1:p.Thr15924Ala
XM_017004820.1:c.43168A>G (TTN)	XP_016860309.1:p.Thr14390Ala
XM_017004821.1:c.43165A>G (TTN)	XP_016860310.1:p.Thr14389Ala
XM_017004822.1:c.40207A>G (TTN)	XP_016860311.1:p.Thr13403Ala
XM_017004823.1:c.21823A>G (TTN)	XP_016860312.1:p.Thr7275Ala
XM_024453094.1:c.43318A>G (TTN)	XP_024308862.1:p.Thr14440Ala
XM_024453095.1:c.43315A>G (TTN)	XP_024308863.1:p.Thr14439Ala
XM_024453096.1:c.42748A>G (TTN)	XP_024308864.1:p.Thr14250Ala
XM_024453097.1:c.40090A>G (TTN)	XP_024308865.1:p.Thr13364Ala
XM_024453098.1:c.40009A>G (TTN)	XP_024308866.1:p.Thr13337Ala
XM_024453099.1:c.21772A>G (TTN)	XP_024308867.1:p.Thr7258Ala
XM_024453100.1:c.11626A>G (TTN)	XP_024308868.1:p.Thr3876Ala