Canonical Allele Identifier: CA349604843

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178568351A>C , CM000664.2:g.178568351A>C	GRCh38
NC_000002.11:g.179433078A>C , CM000664.1:g.179433078A>C	GRCh37
NC_000002.10:g.179141324A>C	NCBI36
NG_011618.3:g.267452T>G , LRG_391:g.267452T>G
NG_051363.1:g.50525A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.77781T>G (TTN) MANE Select	NP_001254479.2:p.Ile25927Met
ENST00000589042.5:c.77781T>G (TTN) MANE Select	ENSP00000467141.1:p.Ile25927Met
NM_001256850.1:c.72858T>G (TTN)	NP_001243779.1:p.Ile24286Met
NM_003319.4:c.50586T>G (TTN)	NP_003310.4:p.Ile16862Met
NM_133378.4:c.70077T>G (TTN)	NP_596869.4:p.Ile23359Met
NM_133432.3:c.50961T>G (TTN)	NP_597676.3:p.Ile16987Met
NM_133437.4:c.51162T>G (TTN)	NP_597681.4:p.Ile17054Met
NR_038271.1:n.447-2949A>C (TTN-AS1)
NR_038272.1:n.2044-14221A>C (TTN-AS1)
ENST00000342175.10:c.51162T>G (TTN)	ENSP00000340554.6:p.Ile17054Met
ENST00000342175.11:c.51162T>G (TTN)	ENSP00000340554.6:p.Ile17054Met
ENST00000342992.10:c.70077T>G (TTN)	ENSP00000343764.6:p.Ile23359Met
ENST00000342992.11:c.70077T>G (TTN)	ENSP00000343764.6:p.Ile23359Met
ENST00000359218.10:c.50961T>G (TTN)	ENSP00000352154.5:p.Ile16987Met
ENST00000359218.9:c.50961T>G (TTN)	ENSP00000352154.5:p.Ile16987Met
ENST00000460472.6:c.50586T>G (TTN)	ENSP00000434586.1:p.Ile16862Met
ENST00000591111.5:c.72858T>G (TTN)	ENSP00000465570.1:p.Ile24286Met
ENST00000615779.4:c.72858T>G (TTN)	ENSP00000483597.1:p.Ile24286Met
XM_011511729.1:c.76878T>G (TTN)	XP_011510031.1:p.Ile25626Met
XM_011511730.1:c.50772T>G (TTN)	XP_011510032.1:p.Ile16924Met
XM_011511731.1:c.50631T>G (TTN)	XP_011510033.1:p.Ile16877Met
XM_017004819.1:c.76674T>G (TTN)	XP_016860308.1:p.Ile25558Met
XM_017004820.1:c.72072T>G (TTN)	XP_016860309.1:p.Ile24024Met
XM_017004821.1:c.72069T>G (TTN)	XP_016860310.1:p.Ile24023Met
XM_017004822.1:c.69111T>G (TTN)	XP_016860311.1:p.Ile23037Met
XM_017004823.1:c.50727T>G (TTN)	XP_016860312.1:p.Ile16909Met
XM_024453094.1:c.72222T>G (TTN)	XP_024308862.1:p.Ile24074Met
XM_024453095.1:c.72219T>G (TTN)	XP_024308863.1:p.Ile24073Met
XM_024453096.1:c.71652T>G (TTN)	XP_024308864.1:p.Ile23884Met
XM_024453097.1:c.68994T>G (TTN)	XP_024308865.1:p.Ile22998Met
XM_024453098.1:c.68913T>G (TTN)	XP_024308866.1:p.Ile22971Met
XM_024453099.1:c.50676T>G (TTN)	XP_024308867.1:p.Ile16892Met
XM_024453100.1:c.40530T>G (TTN)	XP_024308868.1:p.Ile13510Met