Canonical Allele Identifier: CA349445863

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179408004G>C (hg19) ; chr2:g.178543277G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178543277G>C , CM000664.2:g.178543277G>C	GRCh38
NC_000002.11:g.179408004G>C , CM000664.1:g.179408004G>C	GRCh37
NC_000002.10:g.179116250G>C	NCBI36
NG_011618.3:g.292526C>G , LRG_391:g.292526C>G
NG_051363.1:g.25451G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88992C>G (TTN)	ENSP00000343764.6:p.Ser29664Arg
ENST00000342175.11:c.70077C>G (TTN)	ENSP00000340554.6:p.Ser23359Arg
ENST00000359218.10:c.69876C>G (TTN)	ENSP00000352154.5:p.Ser23292Arg
ENST00000342175.10:c.70077C>G (TTN)	ENSP00000340554.6:p.Ser23359Arg
ENST00000342992.10:c.88992C>G (TTN)	ENSP00000343764.6:p.Ser29664Arg
ENST00000359218.9:c.69876C>G (TTN)	ENSP00000352154.5:p.Ser23292Arg
ENST00000460472.6:c.69501C>G (TTN)	ENSP00000434586.1:p.Ser23167Arg
ENST00000589042.5:c.96696C>G (TTN) MANE Select	ENSP00000467141.1:p.Ser32232Arg
ENST00000591111.5:c.91773C>G (TTN)	ENSP00000465570.1:p.Ser30591Arg
ENST00000615779.4:c.91773C>G (TTN)	ENSP00000483597.1:p.Ser30591Arg
NM_001256850.1:c.91773C>G (TTN)	NP_001243779.1:p.Ser30591Arg
NM_001267550.2:c.96696C>G (TTN) MANE Select	NP_001254479.2:p.Ser32232Arg
NM_003319.4:c.69501C>G (TTN)	NP_003310.4:p.Ser23167Arg
NM_133378.4:c.88992C>G (TTN)	NP_596869.4:p.Ser29664Arg
NM_133432.3:c.69876C>G (TTN)	NP_597676.3:p.Ser23292Arg
NM_133437.4:c.70077C>G (TTN)	NP_597681.4:p.Ser23359Arg
NR_038271.1:n.446+19641G>C (TTN-AS1)
NR_038272.1:n.2043+916G>C (TTN-AS1)
XM_011511729.1:c.95793C>G (TTN)	XP_011510031.1:p.Ser31931Arg
XM_011511730.1:c.69687C>G (TTN)	XP_011510032.1:p.Ser23229Arg
XM_011511731.1:c.69546C>G (TTN)	XP_011510033.1:p.Ser23182Arg
XM_017004819.1:c.95589C>G (TTN)	XP_016860308.1:p.Ser31863Arg
XM_017004820.1:c.90987C>G (TTN)	XP_016860309.1:p.Ser30329Arg
XM_017004821.1:c.90984C>G (TTN)	XP_016860310.1:p.Ser30328Arg
XM_017004822.1:c.88026C>G (TTN)	XP_016860311.1:p.Ser29342Arg
XM_017004823.1:c.69642C>G (TTN)	XP_016860312.1:p.Ser23214Arg
XM_024453094.1:c.91137C>G (TTN)	XP_024308862.1:p.Ser30379Arg
XM_024453095.1:c.91134C>G (TTN)	XP_024308863.1:p.Ser30378Arg
XM_024453096.1:c.90567C>G (TTN)	XP_024308864.1:p.Ser30189Arg
XM_024453097.1:c.87909C>G (TTN)	XP_024308865.1:p.Ser29303Arg
XM_024453098.1:c.87828C>G (TTN)	XP_024308866.1:p.Ser29276Arg
XM_024453099.1:c.69591C>G (TTN)	XP_024308867.1:p.Ser23197Arg
XM_024453100.1:c.59445C>G (TTN)	XP_024308868.1:p.Ser19815Arg