Canonical Allele Identifier: CA349411474

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396817G>C (hg19) ; chr2:g.178532090G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532090G>C , CM000664.2:g.178532090G>C	GRCh38
NC_000002.11:g.179396817G>C , CM000664.1:g.179396817G>C	GRCh37
NC_000002.10:g.179105063G>C	NCBI36
NG_011618.3:g.303713C>G , LRG_391:g.303713C>G
NG_051363.1:g.14264G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96821C>G (TTN)	ENSP00000343764.6:p.Ser32274Cys
ENST00000342175.11:c.77906C>G (TTN)	ENSP00000340554.6:p.Ser25969Cys
ENST00000359218.10:c.77705C>G (TTN)	ENSP00000352154.5:p.Ser25902Cys
ENST00000342175.10:c.77906C>G (TTN)	ENSP00000340554.6:p.Ser25969Cys
ENST00000342992.10:c.96821C>G (TTN)	ENSP00000343764.6:p.Ser32274Cys
ENST00000359218.9:c.77705C>G (TTN)	ENSP00000352154.5:p.Ser25902Cys
ENST00000460472.6:c.77330C>G (TTN)	ENSP00000434586.1:p.Ser25777Cys
ENST00000589042.5:c.104525C>G (TTN) MANE Select	ENSP00000467141.1:p.Ser34842Cys
ENST00000591111.5:c.99602C>G (TTN)	ENSP00000465570.1:p.Ser33201Cys
ENST00000615779.4:c.99602C>G (TTN)	ENSP00000483597.1:p.Ser33201Cys
NM_001256850.1:c.99602C>G (TTN)	NP_001243779.1:p.Ser33201Cys
NM_001267550.2:c.104525C>G (TTN) MANE Select	NP_001254479.2:p.Ser34842Cys
NM_003319.4:c.77330C>G (TTN)	NP_003310.4:p.Ser25777Cys
NM_133378.4:c.96821C>G (TTN)	NP_596869.4:p.Ser32274Cys
NM_133432.3:c.77705C>G (TTN)	NP_597676.3:p.Ser25902Cys
NM_133437.4:c.77906C>G (TTN)	NP_597681.4:p.Ser25969Cys
NR_038271.1:n.446+8454G>C (TTN-AS1)
NR_038272.1:n.220-3642G>C (TTN-AS1)
XM_011511729.1:c.103622C>G (TTN)	XP_011510031.1:p.Ser34541Cys
XM_011511730.1:c.77516C>G (TTN)	XP_011510032.1:p.Ser25839Cys
XM_011511731.1:c.77375C>G (TTN)	XP_011510033.1:p.Ser25792Cys
XM_017004819.1:c.103418C>G (TTN)	XP_016860308.1:p.Ser34473Cys
XM_017004820.1:c.98816C>G (TTN)	XP_016860309.1:p.Ser32939Cys
XM_017004821.1:c.98813C>G (TTN)	XP_016860310.1:p.Ser32938Cys
XM_017004822.1:c.95855C>G (TTN)	XP_016860311.1:p.Ser31952Cys
XM_017004823.1:c.77471C>G (TTN)	XP_016860312.1:p.Ser25824Cys
XM_024453094.1:c.98966C>G (TTN)	XP_024308862.1:p.Ser32989Cys
XM_024453095.1:c.98963C>G (TTN)	XP_024308863.1:p.Ser32988Cys
XM_024453096.1:c.98396C>G (TTN)	XP_024308864.1:p.Ser32799Cys
XM_024453097.1:c.95738C>G (TTN)	XP_024308865.1:p.Ser31913Cys
XM_024453098.1:c.95657C>G (TTN)	XP_024308866.1:p.Ser31886Cys
XM_024453099.1:c.77420C>G (TTN)	XP_024308867.1:p.Ser25807Cys
XM_024453100.1:c.67274C>G (TTN)	XP_024308868.1:p.Ser22425Cys