Canonical Allele Identifier: CA349405801

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179394975T>C (hg19) ; chr2:g.178530248T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530248T>C , CM000664.2:g.178530248T>C	GRCh38
NC_000002.11:g.179394975T>C , CM000664.1:g.179394975T>C	GRCh37
NC_000002.10:g.179103221T>C	NCBI36
NG_011618.3:g.305555A>G , LRG_391:g.305555A>G
NG_051363.1:g.12422T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98663A>G (TTN)	ENSP00000343764.6:p.Asp32888Gly
ENST00000342175.11:c.79748A>G (TTN)	ENSP00000340554.6:p.Asp26583Gly
ENST00000359218.10:c.79547A>G (TTN)	ENSP00000352154.5:p.Asp26516Gly
ENST00000342175.10:c.79748A>G (TTN)	ENSP00000340554.6:p.Asp26583Gly
ENST00000342992.10:c.98663A>G (TTN)	ENSP00000343764.6:p.Asp32888Gly
ENST00000359218.9:c.79547A>G (TTN)	ENSP00000352154.5:p.Asp26516Gly
ENST00000460472.6:c.79172A>G (TTN)	ENSP00000434586.1:p.Asp26391Gly
ENST00000589042.5:c.106367A>G (TTN) MANE Select	ENSP00000467141.1:p.Asp35456Gly
ENST00000591111.5:c.101444A>G (TTN)	ENSP00000465570.1:p.Asp33815Gly
ENST00000615779.4:c.101444A>G (TTN)	ENSP00000483597.1:p.Asp33815Gly
NM_001256850.1:c.101444A>G (TTN)	NP_001243779.1:p.Asp33815Gly
NM_001267550.2:c.106367A>G (TTN) MANE Select	NP_001254479.2:p.Asp35456Gly
NM_003319.4:c.79172A>G (TTN)	NP_003310.4:p.Asp26391Gly
NM_133378.4:c.98663A>G (TTN)	NP_596869.4:p.Asp32888Gly
NM_133432.3:c.79547A>G (TTN)	NP_597676.3:p.Asp26516Gly
NM_133437.4:c.79748A>G (TTN)	NP_597681.4:p.Asp26583Gly
NR_038271.1:n.446+6612T>C (TTN-AS1)
NR_038272.1:n.220-5484T>C (TTN-AS1)
XM_011511729.1:c.105464A>G (TTN)	XP_011510031.1:p.Asp35155Gly
XM_011511730.1:c.79358A>G (TTN)	XP_011510032.1:p.Asp26453Gly
XM_011511731.1:c.79217A>G (TTN)	XP_011510033.1:p.Asp26406Gly
XM_017004819.1:c.105260A>G (TTN)	XP_016860308.1:p.Asp35087Gly
XM_017004820.1:c.100658A>G (TTN)	XP_016860309.1:p.Asp33553Gly
XM_017004821.1:c.100655A>G (TTN)	XP_016860310.1:p.Asp33552Gly
XM_017004822.1:c.97697A>G (TTN)	XP_016860311.1:p.Asp32566Gly
XM_017004823.1:c.79313A>G (TTN)	XP_016860312.1:p.Asp26438Gly
XM_024453094.1:c.100808A>G (TTN)	XP_024308862.1:p.Asp33603Gly
XM_024453095.1:c.100805A>G (TTN)	XP_024308863.1:p.Asp33602Gly
XM_024453096.1:c.100238A>G (TTN)	XP_024308864.1:p.Asp33413Gly
XM_024453097.1:c.97580A>G (TTN)	XP_024308865.1:p.Asp32527Gly
XM_024453098.1:c.97499A>G (TTN)	XP_024308866.1:p.Asp32500Gly
XM_024453099.1:c.79262A>G (TTN)	XP_024308867.1:p.Asp26421Gly
XM_024453100.1:c.69116A>G (TTN)	XP_024308868.1:p.Asp23039Gly