Canonical Allele Identifier: CA60969988

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543528T>C , CM000664.2:g.178543528T>C	GRCh38
NC_000002.11:g.179408255T>C , CM000664.1:g.179408255T>C	GRCh37
NC_000002.10:g.179116501T>C	NCBI36
NG_011618.3:g.292275A>G , LRG_391:g.292275A>G
NG_051363.1:g.25702T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.96445A>G (TTN) MANE Select	NP_001254479.2:p.Met32149Val
ENST00000589042.5:c.96445A>G (TTN) MANE Select	ENSP00000467141.1:p.Met32149Val
NM_001256850.1:c.91522A>G (TTN)	NP_001243779.1:p.Met30508Val
NM_003319.4:c.69250A>G (TTN)	NP_003310.4:p.Met23084Val
NM_133378.4:c.88741A>G (TTN)	NP_596869.4:p.Met29581Val
NM_133432.3:c.69625A>G (TTN)	NP_597676.3:p.Met23209Val
NM_133437.4:c.69826A>G (TTN)	NP_597681.4:p.Met23276Val
NR_038271.1:n.446+19892T>C (TTN-AS1)
NR_038272.1:n.2043+1167T>C (TTN-AS1)
ENST00000342175.10:c.69826A>G (TTN)	ENSP00000340554.6:p.Met23276Val
ENST00000342175.11:c.69826A>G (TTN)	ENSP00000340554.6:p.Met23276Val
ENST00000342992.10:c.88741A>G (TTN)	ENSP00000343764.6:p.Met29581Val
ENST00000342992.11:c.88741A>G (TTN)	ENSP00000343764.6:p.Met29581Val
ENST00000359218.10:c.69625A>G (TTN)	ENSP00000352154.5:p.Met23209Val
ENST00000359218.9:c.69625A>G (TTN)	ENSP00000352154.5:p.Met23209Val
ENST00000460472.6:c.69250A>G (TTN)	ENSP00000434586.1:p.Met23084Val
ENST00000591111.5:c.91522A>G (TTN)	ENSP00000465570.1:p.Met30508Val
ENST00000615779.4:c.91522A>G (TTN)	ENSP00000483597.1:p.Met30508Val
XM_011511729.1:c.95542A>G (TTN)	XP_011510031.1:p.Met31848Val
XM_011511730.1:c.69436A>G (TTN)	XP_011510032.1:p.Met23146Val
XM_011511731.1:c.69295A>G (TTN)	XP_011510033.1:p.Met23099Val
XM_017004819.1:c.95338A>G (TTN)	XP_016860308.1:p.Met31780Val
XM_017004820.1:c.90736A>G (TTN)	XP_016860309.1:p.Met30246Val
XM_017004821.1:c.90733A>G (TTN)	XP_016860310.1:p.Met30245Val
XM_017004822.1:c.87775A>G (TTN)	XP_016860311.1:p.Met29259Val
XM_017004823.1:c.69391A>G (TTN)	XP_016860312.1:p.Met23131Val
XM_024453094.1:c.90886A>G (TTN)	XP_024308862.1:p.Met30296Val
XM_024453095.1:c.90883A>G (TTN)	XP_024308863.1:p.Met30295Val
XM_024453096.1:c.90316A>G (TTN)	XP_024308864.1:p.Met30106Val
XM_024453097.1:c.87658A>G (TTN)	XP_024308865.1:p.Met29220Val
XM_024453098.1:c.87577A>G (TTN)	XP_024308866.1:p.Met29193Val
XM_024453099.1:c.69340A>G (TTN)	XP_024308867.1:p.Met23114Val
XM_024453100.1:c.59194A>G (TTN)	XP_024308868.1:p.Met19732Val