Canonical Allele Identifier: CA60970476

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs371741687
• gnomAD v2: 2-179408907-A-G
• gnomAD v3: 2-178544180-A-G
• gnomAD v4: 2-178544180-A-G
• MyVariant Identifiers: chr2:g.179408907A>G (hg19) ; chr2:g.178544180A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544180A>G , CM000664.2:g.178544180A>G	GRCh38
NC_000002.11:g.179408907A>G , CM000664.1:g.179408907A>G	GRCh37
NC_000002.10:g.179117153A>G	NCBI36
NG_011618.3:g.291623T>C , LRG_391:g.291623T>C
NG_051363.1:g.26354A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88324+21T>C (TTN)	ENSP00000343764.6:n.88324+21T>C
ENST00000342175.11:c.69409+21T>C (TTN)	ENSP00000340554.6:n.69409+21T>C
ENST00000359218.10:c.69208+21T>C (TTN)	ENSP00000352154.5:n.69208+21T>C
ENST00000342175.10:c.69409+21T>C (TTN)	ENSP00000340554.6:n.69409+21T>C
ENST00000342992.10:c.88324+21T>C (TTN)	ENSP00000343764.6:n.88324+21T>C
ENST00000359218.9:c.69208+21T>C (TTN)	ENSP00000352154.5:n.69208+21T>C
ENST00000460472.6:c.68833+21T>C (TTN)	ENSP00000434586.1:n.68833+21T>C
ENST00000589042.5:c.96028+21T>C (TTN) MANE Select	ENSP00000467141.1:n.96028+21T>C
ENST00000591111.5:c.91105+21T>C (TTN)	ENSP00000465570.1:n.91105+21T>C
ENST00000615779.4:c.91105+21T>C (TTN)	ENSP00000483597.1:n.91105+21T>C
NM_001256850.1:c.91105+21T>C (TTN)	NP_001243779.1:n.91105+21T>C
NM_001267550.2:c.96028+21T>C (TTN) MANE Select	NP_001254479.2:n.96028+21T>C
NM_003319.4:c.68833+21T>C (TTN)	NP_003310.4:n.68833+21T>C
NM_133378.4:c.88324+21T>C (TTN)	NP_596869.4:n.88324+21T>C
NM_133432.3:c.69208+21T>C (TTN)	NP_597676.3:n.69208+21T>C
NM_133437.4:c.69409+21T>C (TTN)	NP_597681.4:n.69409+21T>C
NR_038271.1:n.446+20544A>G (TTN-AS1)
NR_038272.1:n.2043+1819A>G (TTN-AS1)
XM_011511729.1:c.95125+21T>C (TTN)	XP_011510031.1:n.95125+21T>C
XM_011511730.1:c.69019+21T>C (TTN)	XP_011510032.1:n.69019+21T>C
XM_011511731.1:c.68878+21T>C (TTN)	XP_011510033.1:n.68878+21T>C
XM_017004819.1:c.94921+21T>C (TTN)	XP_016860308.1:n.94921+21T>C
XM_017004820.1:c.90319+21T>C (TTN)	XP_016860309.1:n.90319+21T>C
XM_017004821.1:c.90316+21T>C (TTN)	XP_016860310.1:n.90316+21T>C
XM_017004822.1:c.87358+21T>C (TTN)	XP_016860311.1:n.87358+21T>C
XM_017004823.1:c.68974+21T>C (TTN)	XP_016860312.1:n.68974+21T>C
XM_024453094.1:c.90469+21T>C (TTN)	XP_024308862.1:n.90469+21T>C
XM_024453095.1:c.90466+21T>C (TTN)	XP_024308863.1:n.90466+21T>C
XM_024453096.1:c.89899+21T>C (TTN)	XP_024308864.1:n.89899+21T>C
XM_024453097.1:c.87241+21T>C (TTN)	XP_024308865.1:n.87241+21T>C
XM_024453098.1:c.87160+21T>C (TTN)	XP_024308866.1:n.87160+21T>C
XM_024453099.1:c.68923+21T>C (TTN)	XP_024308867.1:n.68923+21T>C
XM_024453100.1:c.58777+21T>C (TTN)	XP_024308868.1:n.58777+21T>C