Canonical Allele Identifier: CA349427703

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179402255C>A (hg19) ; chr2:g.178537528C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178537528C>A , CM000664.2:g.178537528C>A	GRCh38
NC_000002.11:g.179402255C>A , CM000664.1:g.179402255C>A	GRCh37
NC_000002.10:g.179110501C>A	NCBI36
NG_011618.3:g.298275G>T , LRG_391:g.298275G>T
NG_051363.1:g.19702C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.91975G>T (TTN)	ENSP00000343764.6:p.Ala30659Ser
ENST00000342175.11:c.73060G>T (TTN)	ENSP00000340554.6:p.Ala24354Ser
ENST00000359218.10:c.72859G>T (TTN)	ENSP00000352154.5:p.Ala24287Ser
ENST00000342175.10:c.73060G>T (TTN)	ENSP00000340554.6:p.Ala24354Ser
ENST00000342992.10:c.91975G>T (TTN)	ENSP00000343764.6:p.Ala30659Ser
ENST00000359218.9:c.72859G>T (TTN)	ENSP00000352154.5:p.Ala24287Ser
ENST00000460472.6:c.72484G>T (TTN)	ENSP00000434586.1:p.Ala24162Ser
ENST00000589042.5:c.99679G>T (TTN) MANE Select	ENSP00000467141.1:p.Ala33227Ser
ENST00000591111.5:c.94756G>T (TTN)	ENSP00000465570.1:p.Ala31586Ser
ENST00000615779.4:c.94756G>T (TTN)	ENSP00000483597.1:p.Ala31586Ser
NM_001256850.1:c.94756G>T (TTN)	NP_001243779.1:p.Ala31586Ser
NM_001267550.2:c.99679G>T (TTN) MANE Select	NP_001254479.2:p.Ala33227Ser
NM_003319.4:c.72484G>T (TTN)	NP_003310.4:p.Ala24162Ser
NM_133378.4:c.91975G>T (TTN)	NP_596869.4:p.Ala30659Ser
NM_133432.3:c.72859G>T (TTN)	NP_597676.3:p.Ala24287Ser
NM_133437.4:c.73060G>T (TTN)	NP_597681.4:p.Ala24354Ser
NR_038271.1:n.446+13892C>A (TTN-AS1)
NR_038272.1:n.484C>A (TTN-AS1)
XM_011511729.1:c.98776G>T (TTN)	XP_011510031.1:p.Ala32926Ser
XM_011511730.1:c.72670G>T (TTN)	XP_011510032.1:p.Ala24224Ser
XM_011511731.1:c.72529G>T (TTN)	XP_011510033.1:p.Ala24177Ser
XM_017004819.1:c.98572G>T (TTN)	XP_016860308.1:p.Ala32858Ser
XM_017004820.1:c.93970G>T (TTN)	XP_016860309.1:p.Ala31324Ser
XM_017004821.1:c.93967G>T (TTN)	XP_016860310.1:p.Ala31323Ser
XM_017004822.1:c.91009G>T (TTN)	XP_016860311.1:p.Ala30337Ser
XM_017004823.1:c.72625G>T (TTN)	XP_016860312.1:p.Ala24209Ser
XM_024453094.1:c.94120G>T (TTN)	XP_024308862.1:p.Ala31374Ser
XM_024453095.1:c.94117G>T (TTN)	XP_024308863.1:p.Ala31373Ser
XM_024453096.1:c.93550G>T (TTN)	XP_024308864.1:p.Ala31184Ser
XM_024453097.1:c.90892G>T (TTN)	XP_024308865.1:p.Ala30298Ser
XM_024453098.1:c.90811G>T (TTN)	XP_024308866.1:p.Ala30271Ser
XM_024453099.1:c.72574G>T (TTN)	XP_024308867.1:p.Ala24192Ser
XM_024453100.1:c.62428G>T (TTN)	XP_024308868.1:p.Ala20810Ser