Canonical Allele Identifier: CA1310521367

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs1695923707
• gnomAD v4: 2-178544149-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544149T>C , CM000664.2:g.178544149T>C	GRCh38
NC_000002.11:g.179408876T>C , CM000664.1:g.179408876T>C	GRCh37
NC_000002.10:g.179117122T>C	NCBI36
NG_011618.3:g.291654A>G , LRG_391:g.291654A>G
NG_051363.1:g.26323T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88325-34A>G (TTN)	ENSP00000343764.6:n.88325-34A>G
ENST00000342175.11:c.69410-34A>G (TTN)	ENSP00000340554.6:n.69410-34A>G
ENST00000359218.10:c.69209-34A>G (TTN)	ENSP00000352154.5:n.69209-34A>G
ENST00000342175.10:c.69410-34A>G (TTN)	ENSP00000340554.6:n.69410-34A>G
ENST00000342992.10:c.88325-34A>G (TTN)	ENSP00000343764.6:n.88325-34A>G
ENST00000359218.9:c.69209-34A>G (TTN)	ENSP00000352154.5:n.69209-34A>G
ENST00000460472.6:c.68834-34A>G (TTN)	ENSP00000434586.1:n.68834-34A>G
ENST00000589042.5:c.96029-34A>G (TTN) MANE Select	ENSP00000467141.1:n.96029-34A>G
ENST00000591111.5:c.91106-34A>G (TTN)	ENSP00000465570.1:n.91106-34A>G
ENST00000615779.4:c.91106-34A>G (TTN)	ENSP00000483597.1:n.91106-34A>G
NM_001256850.1:c.91106-34A>G (TTN)	NP_001243779.1:n.91106-34A>G
NM_001267550.2:c.96029-34A>G (TTN) MANE Select	NP_001254479.2:n.96029-34A>G
NM_003319.4:c.68834-34A>G (TTN)	NP_003310.4:n.68834-34A>G
NM_133378.4:c.88325-34A>G (TTN)	NP_596869.4:n.88325-34A>G
NM_133432.3:c.69209-34A>G (TTN)	NP_597676.3:n.69209-34A>G
NM_133437.4:c.69410-34A>G (TTN)	NP_597681.4:n.69410-34A>G
NR_038271.1:n.446+20513T>C (TTN-AS1)
NR_038272.1:n.2043+1788T>C (TTN-AS1)
XM_011511729.1:c.95126-34A>G (TTN)	XP_011510031.1:n.95126-34A>G
XM_011511730.1:c.69020-34A>G (TTN)	XP_011510032.1:n.69020-34A>G
XM_011511731.1:c.68879-34A>G (TTN)	XP_011510033.1:n.68879-34A>G
XM_017004819.1:c.94922-34A>G (TTN)	XP_016860308.1:n.94922-34A>G
XM_017004820.1:c.90320-34A>G (TTN)	XP_016860309.1:n.90320-34A>G
XM_017004821.1:c.90317-34A>G (TTN)	XP_016860310.1:n.90317-34A>G
XM_017004822.1:c.87359-34A>G (TTN)	XP_016860311.1:n.87359-34A>G
XM_017004823.1:c.68975-34A>G (TTN)	XP_016860312.1:n.68975-34A>G
XM_024453094.1:c.90470-34A>G (TTN)	XP_024308862.1:n.90470-34A>G
XM_024453095.1:c.90467-34A>G (TTN)	XP_024308863.1:n.90467-34A>G
XM_024453096.1:c.89900-34A>G (TTN)	XP_024308864.1:n.89900-34A>G
XM_024453097.1:c.87242-34A>G (TTN)	XP_024308865.1:n.87242-34A>G
XM_024453098.1:c.87161-34A>G (TTN)	XP_024308866.1:n.87161-34A>G
XM_024453099.1:c.68924-34A>G (TTN)	XP_024308867.1:n.68924-34A>G
XM_024453100.1:c.58778-34A>G (TTN)	XP_024308868.1:n.58778-34A>G