Canonical Allele Identifier: CA2662125441

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178540050-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178540050A>C , CM000664.2:g.178540050A>C	GRCh38
NC_000002.11:g.179404777A>C , CM000664.1:g.179404777A>C	GRCh37
NC_000002.10:g.179113023A>C	NCBI36
NG_011618.3:g.295753T>G , LRG_391:g.295753T>G
NG_051363.1:g.22224A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.90394+18T>G (TTN)	ENSP00000343764.6:n.90394+18T>G
ENST00000342175.11:c.71479+18T>G (TTN)	ENSP00000340554.6:n.71479+18T>G
ENST00000359218.10:c.71278+18T>G (TTN)	ENSP00000352154.5:n.71278+18T>G
ENST00000342175.10:c.71479+18T>G (TTN)	ENSP00000340554.6:n.71479+18T>G
ENST00000342992.10:c.90394+18T>G (TTN)	ENSP00000343764.6:n.90394+18T>G
ENST00000359218.9:c.71278+18T>G (TTN)	ENSP00000352154.5:n.71278+18T>G
ENST00000460472.6:c.70903+18T>G (TTN)	ENSP00000434586.1:n.70903+18T>G
ENST00000589042.5:c.98098+18T>G (TTN) MANE Select	ENSP00000467141.1:n.98098+18T>G
ENST00000591111.5:c.93175+18T>G (TTN)	ENSP00000465570.1:n.93175+18T>G
ENST00000615779.4:c.93175+18T>G (TTN)	ENSP00000483597.1:n.93175+18T>G
NM_001256850.1:c.93175+18T>G (TTN)	NP_001243779.1:n.93175+18T>G
NM_001267550.2:c.98098+18T>G (TTN) MANE Select	NP_001254479.2:n.98098+18T>G
NM_003319.4:c.70903+18T>G (TTN)	NP_003310.4:n.70903+18T>G
NM_133378.4:c.90394+18T>G (TTN)	NP_596869.4:n.90394+18T>G
NM_133432.3:c.71278+18T>G (TTN)	NP_597676.3:n.71278+18T>G
NM_133437.4:c.71479+18T>G (TTN)	NP_597681.4:n.71479+18T>G
NR_038271.1:n.446+16414A>C (TTN-AS1)
NR_038272.1:n.1841-57A>C (TTN-AS1)
XM_011511729.1:c.97195+18T>G (TTN)	XP_011510031.1:n.97195+18T>G
XM_011511730.1:c.71089+18T>G (TTN)	XP_011510032.1:n.71089+18T>G
XM_011511731.1:c.70948+18T>G (TTN)	XP_011510033.1:n.70948+18T>G
XM_017004819.1:c.96991+18T>G (TTN)	XP_016860308.1:n.96991+18T>G
XM_017004820.1:c.92389+18T>G (TTN)	XP_016860309.1:n.92389+18T>G
XM_017004821.1:c.92386+18T>G (TTN)	XP_016860310.1:n.92386+18T>G
XM_017004822.1:c.89428+18T>G (TTN)	XP_016860311.1:n.89428+18T>G
XM_017004823.1:c.71044+18T>G (TTN)	XP_016860312.1:n.71044+18T>G
XM_024453094.1:c.92539+18T>G (TTN)	XP_024308862.1:n.92539+18T>G
XM_024453095.1:c.92536+18T>G (TTN)	XP_024308863.1:n.92536+18T>G
XM_024453096.1:c.91969+18T>G (TTN)	XP_024308864.1:n.91969+18T>G
XM_024453097.1:c.89311+18T>G (TTN)	XP_024308865.1:n.89311+18T>G
XM_024453098.1:c.89230+18T>G (TTN)	XP_024308866.1:n.89230+18T>G
XM_024453099.1:c.70993+18T>G (TTN)	XP_024308867.1:n.70993+18T>G
XM_024453100.1:c.60847+18T>G (TTN)	XP_024308868.1:n.60847+18T>G