Canonical Allele Identifier: CA349398659

Gene: TTN TTN-AS1

Linked Data

• COSMIC: COSM4087109 ; COSM4087110 ; COSM4087111 ; COSM4087112
• MyVariant Identifiers: chr2:g.179391860T>C (hg19) ; chr2:g.178527133T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178527133T>C , CM000664.2:g.178527133T>C	GRCh38
NC_000002.11:g.179391860T>C , CM000664.1:g.179391860T>C	GRCh37
NC_000002.10:g.179100106T>C	NCBI36
NG_011618.3:g.308670A>G , LRG_391:g.308670A>G
NG_051363.1:g.9307T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.100151A>G (TTN)	ENSP00000343764.6:p.Asp33384Gly
ENST00000342175.11:c.81236A>G (TTN)	ENSP00000340554.6:p.Asp27079Gly
ENST00000359218.10:c.81035A>G (TTN)	ENSP00000352154.5:p.Asp27012Gly
ENST00000342175.10:c.81236A>G (TTN)	ENSP00000340554.6:p.Asp27079Gly
ENST00000342992.10:c.100151A>G (TTN)	ENSP00000343764.6:p.Asp33384Gly
ENST00000359218.9:c.81035A>G (TTN)	ENSP00000352154.5:p.Asp27012Gly
ENST00000460472.6:c.80660A>G (TTN)	ENSP00000434586.1:p.Asp26887Gly
ENST00000589042.5:c.107855A>G (TTN) MANE Select	ENSP00000467141.1:p.Asp35952Gly
ENST00000591111.5:c.102932A>G (TTN)	ENSP00000465570.1:p.Asp34311Gly
ENST00000615779.4:c.102932A>G (TTN)	ENSP00000483597.1:p.Asp34311Gly
NM_001256850.1:c.102932A>G (TTN)	NP_001243779.1:p.Asp34311Gly
NM_001267550.2:c.107855A>G (TTN) MANE Select	NP_001254479.2:p.Asp35952Gly
NM_003319.4:c.80660A>G (TTN)	NP_003310.4:p.Asp26887Gly
NM_133378.4:c.100151A>G (TTN)	NP_596869.4:p.Asp33384Gly
NM_133432.3:c.81035A>G (TTN)	NP_597676.3:p.Asp27012Gly
NM_133437.4:c.81236A>G (TTN)	NP_597681.4:p.Asp27079Gly
NR_038271.1:n.446+3497T>C (TTN-AS1)
NR_038272.1:n.219+3497T>C (TTN-AS1)
XM_011511729.1:c.106952A>G (TTN)	XP_011510031.1:p.Asp35651Gly
XM_011511730.1:c.80846A>G (TTN)	XP_011510032.1:p.Asp26949Gly
XM_011511731.1:c.80705A>G (TTN)	XP_011510033.1:p.Asp26902Gly
XM_017004819.1:c.106748A>G (TTN)	XP_016860308.1:p.Asp35583Gly
XM_017004820.1:c.102146A>G (TTN)	XP_016860309.1:p.Asp34049Gly
XM_017004821.1:c.102143A>G (TTN)	XP_016860310.1:p.Asp34048Gly
XM_017004822.1:c.99185A>G (TTN)	XP_016860311.1:p.Asp33062Gly
XM_017004823.1:c.80801A>G (TTN)	XP_016860312.1:p.Asp26934Gly
XM_024453094.1:c.102296A>G (TTN)	XP_024308862.1:p.Asp34099Gly
XM_024453095.1:c.102293A>G (TTN)	XP_024308863.1:p.Asp34098Gly
XM_024453096.1:c.101726A>G (TTN)	XP_024308864.1:p.Asp33909Gly
XM_024453097.1:c.99068A>G (TTN)	XP_024308865.1:p.Asp33023Gly
XM_024453098.1:c.98987A>G (TTN)	XP_024308866.1:p.Asp32996Gly
XM_024453099.1:c.80750A>G (TTN)	XP_024308867.1:p.Asp26917Gly
XM_024453100.1:c.70604A>G (TTN)	XP_024308868.1:p.Asp23535Gly