Canonical Allele Identifier: CA349405194

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178530033-G-C
• MyVariant Identifiers: chr2:g.179394760G>C (hg19) ; chr2:g.178530033G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530033G>C , CM000664.2:g.178530033G>C	GRCh38
NC_000002.11:g.179394760G>C , CM000664.1:g.179394760G>C	GRCh37
NC_000002.10:g.179103006G>C	NCBI36
NG_011618.3:g.305770C>G , LRG_391:g.305770C>G
NG_051363.1:g.12207G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98754C>G (TTN)	ENSP00000343764.6:p.Asp32918Glu
ENST00000342175.11:c.79839C>G (TTN)	ENSP00000340554.6:p.Asp26613Glu
ENST00000359218.10:c.79638C>G (TTN)	ENSP00000352154.5:p.Asp26546Glu
ENST00000342175.10:c.79839C>G (TTN)	ENSP00000340554.6:p.Asp26613Glu
ENST00000342992.10:c.98754C>G (TTN)	ENSP00000343764.6:p.Asp32918Glu
ENST00000359218.9:c.79638C>G (TTN)	ENSP00000352154.5:p.Asp26546Glu
ENST00000460472.6:c.79263C>G (TTN)	ENSP00000434586.1:p.Asp26421Glu
ENST00000589042.5:c.106458C>G (TTN) MANE Select	ENSP00000467141.1:p.Asp35486Glu
ENST00000591111.5:c.101535C>G (TTN)	ENSP00000465570.1:p.Asp33845Glu
ENST00000615779.4:c.101535C>G (TTN)	ENSP00000483597.1:p.Asp33845Glu
NM_001256850.1:c.101535C>G (TTN)	NP_001243779.1:p.Asp33845Glu
NM_001267550.2:c.106458C>G (TTN) MANE Select	NP_001254479.2:p.Asp35486Glu
NM_003319.4:c.79263C>G (TTN)	NP_003310.4:p.Asp26421Glu
NM_133378.4:c.98754C>G (TTN)	NP_596869.4:p.Asp32918Glu
NM_133432.3:c.79638C>G (TTN)	NP_597676.3:p.Asp26546Glu
NM_133437.4:c.79839C>G (TTN)	NP_597681.4:p.Asp26613Glu
NR_038271.1:n.446+6397G>C (TTN-AS1)
NR_038272.1:n.220-5699G>C (TTN-AS1)
XM_011511729.1:c.105555C>G (TTN)	XP_011510031.1:p.Asp35185Glu
XM_011511730.1:c.79449C>G (TTN)	XP_011510032.1:p.Asp26483Glu
XM_011511731.1:c.79308C>G (TTN)	XP_011510033.1:p.Asp26436Glu
XM_017004819.1:c.105351C>G (TTN)	XP_016860308.1:p.Asp35117Glu
XM_017004820.1:c.100749C>G (TTN)	XP_016860309.1:p.Asp33583Glu
XM_017004821.1:c.100746C>G (TTN)	XP_016860310.1:p.Asp33582Glu
XM_017004822.1:c.97788C>G (TTN)	XP_016860311.1:p.Asp32596Glu
XM_017004823.1:c.79404C>G (TTN)	XP_016860312.1:p.Asp26468Glu
XM_024453094.1:c.100899C>G (TTN)	XP_024308862.1:p.Asp33633Glu
XM_024453095.1:c.100896C>G (TTN)	XP_024308863.1:p.Asp33632Glu
XM_024453096.1:c.100329C>G (TTN)	XP_024308864.1:p.Asp33443Glu
XM_024453097.1:c.97671C>G (TTN)	XP_024308865.1:p.Asp32557Glu
XM_024453098.1:c.97590C>G (TTN)	XP_024308866.1:p.Asp32530Glu
XM_024453099.1:c.79353C>G (TTN)	XP_024308867.1:p.Asp26451Glu
XM_024453100.1:c.69207C>G (TTN)	XP_024308868.1:p.Asp23069Glu