Canonical Allele Identifier: CA349503341

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179416467G>C (hg19) ; chr2:g.178551740G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178551740G>C , CM000664.2:g.178551740G>C	GRCh38
NC_000002.11:g.179416467G>C , CM000664.1:g.179416467G>C	GRCh37
NC_000002.10:g.179124713G>C	NCBI36
NG_011618.3:g.284063C>G , LRG_391:g.284063C>G
NG_051363.1:g.33914G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.83456C>G (TTN)	ENSP00000343764.6:p.Thr27819Ser
ENST00000342175.11:c.64541C>G (TTN)	ENSP00000340554.6:p.Thr21514Ser
ENST00000359218.10:c.64340C>G (TTN)	ENSP00000352154.5:p.Thr21447Ser
ENST00000342175.10:c.64541C>G (TTN)	ENSP00000340554.6:p.Thr21514Ser
ENST00000342992.10:c.83456C>G (TTN)	ENSP00000343764.6:p.Thr27819Ser
ENST00000359218.9:c.64340C>G (TTN)	ENSP00000352154.5:p.Thr21447Ser
ENST00000460472.6:c.63965C>G (TTN)	ENSP00000434586.1:p.Thr21322Ser
ENST00000589042.5:c.91160C>G (TTN) MANE Select	ENSP00000467141.1:p.Thr30387Ser
ENST00000591111.5:c.86237C>G (TTN)	ENSP00000465570.1:p.Thr28746Ser
ENST00000615779.4:c.86237C>G (TTN)	ENSP00000483597.1:p.Thr28746Ser
NM_001256850.1:c.86237C>G (TTN)	NP_001243779.1:p.Thr28746Ser
NM_001267550.2:c.91160C>G (TTN) MANE Select	NP_001254479.2:p.Thr30387Ser
NM_003319.4:c.63965C>G (TTN)	NP_003310.4:p.Thr21322Ser
NM_133378.4:c.83456C>G (TTN)	NP_596869.4:p.Thr27819Ser
NM_133432.3:c.64340C>G (TTN)	NP_597676.3:p.Thr21447Ser
NM_133437.4:c.64541C>G (TTN)	NP_597681.4:p.Thr21514Ser
NR_038271.1:n.447-19560G>C (TTN-AS1)
NR_038272.1:n.2043+9379G>C (TTN-AS1)
XM_011511729.1:c.90257C>G (TTN)	XP_011510031.1:p.Thr30086Ser
XM_011511730.1:c.64151C>G (TTN)	XP_011510032.1:p.Thr21384Ser
XM_011511731.1:c.64010C>G (TTN)	XP_011510033.1:p.Thr21337Ser
XM_017004819.1:c.90053C>G (TTN)	XP_016860308.1:p.Thr30018Ser
XM_017004820.1:c.85451C>G (TTN)	XP_016860309.1:p.Thr28484Ser
XM_017004821.1:c.85448C>G (TTN)	XP_016860310.1:p.Thr28483Ser
XM_017004822.1:c.82490C>G (TTN)	XP_016860311.1:p.Thr27497Ser
XM_017004823.1:c.64106C>G (TTN)	XP_016860312.1:p.Thr21369Ser
XM_024453094.1:c.85601C>G (TTN)	XP_024308862.1:p.Thr28534Ser
XM_024453095.1:c.85598C>G (TTN)	XP_024308863.1:p.Thr28533Ser
XM_024453096.1:c.85031C>G (TTN)	XP_024308864.1:p.Thr28344Ser
XM_024453097.1:c.82373C>G (TTN)	XP_024308865.1:p.Thr27458Ser
XM_024453098.1:c.82292C>G (TTN)	XP_024308866.1:p.Thr27431Ser
XM_024453099.1:c.64055C>G (TTN)	XP_024308867.1:p.Thr21352Ser
XM_024453100.1:c.53909C>G (TTN)	XP_024308868.1:p.Thr17970Ser