Canonical Allele Identifier: CA349620946

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179435176G>C (hg19) ; chr2:g.178570449G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178570449G>C , CM000664.2:g.178570449G>C	GRCh38
NC_000002.11:g.179435176G>C , CM000664.1:g.179435176G>C	GRCh37
NC_000002.10:g.179143422G>C	NCBI36
NG_011618.3:g.265354C>G , LRG_391:g.265354C>G
NG_051363.1:g.52623G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.67979C>G (TTN)	ENSP00000343764.6:p.Pro22660Arg
ENST00000342175.11:c.49064C>G (TTN)	ENSP00000340554.6:p.Pro16355Arg
ENST00000359218.10:c.48863C>G (TTN)	ENSP00000352154.5:p.Pro16288Arg
ENST00000342175.10:c.49064C>G (TTN)	ENSP00000340554.6:p.Pro16355Arg
ENST00000342992.10:c.67979C>G (TTN)	ENSP00000343764.6:p.Pro22660Arg
ENST00000359218.9:c.48863C>G (TTN)	ENSP00000352154.5:p.Pro16288Arg
ENST00000460472.6:c.48488C>G (TTN)	ENSP00000434586.1:p.Pro16163Arg
ENST00000589042.5:c.75683C>G (TTN) MANE Select	ENSP00000467141.1:p.Pro25228Arg
ENST00000591111.5:c.70760C>G (TTN)	ENSP00000465570.1:p.Pro23587Arg
ENST00000615779.4:c.70760C>G (TTN)	ENSP00000483597.1:p.Pro23587Arg
NM_001256850.1:c.70760C>G (TTN)	NP_001243779.1:p.Pro23587Arg
NM_001267550.2:c.75683C>G (TTN) MANE Select	NP_001254479.2:p.Pro25228Arg
NM_003319.4:c.48488C>G (TTN)	NP_003310.4:p.Pro16163Arg
NM_133378.4:c.67979C>G (TTN)	NP_596869.4:p.Pro22660Arg
NM_133432.3:c.48863C>G (TTN)	NP_597676.3:p.Pro16288Arg
NM_133437.4:c.49064C>G (TTN)	NP_597681.4:p.Pro16355Arg
NR_038271.1:n.447-851G>C (TTN-AS1)
NR_038272.1:n.2044-12123G>C (TTN-AS1)
XM_011511729.1:c.74780C>G (TTN)	XP_011510031.1:p.Pro24927Arg
XM_011511730.1:c.48674C>G (TTN)	XP_011510032.1:p.Pro16225Arg
XM_011511731.1:c.48533C>G (TTN)	XP_011510033.1:p.Pro16178Arg
XM_017004819.1:c.74576C>G (TTN)	XP_016860308.1:p.Pro24859Arg
XM_017004820.1:c.69974C>G (TTN)	XP_016860309.1:p.Pro23325Arg
XM_017004821.1:c.69971C>G (TTN)	XP_016860310.1:p.Pro23324Arg
XM_017004822.1:c.67013C>G (TTN)	XP_016860311.1:p.Pro22338Arg
XM_017004823.1:c.48629C>G (TTN)	XP_016860312.1:p.Pro16210Arg
XM_024453094.1:c.70124C>G (TTN)	XP_024308862.1:p.Pro23375Arg
XM_024453095.1:c.70121C>G (TTN)	XP_024308863.1:p.Pro23374Arg
XM_024453096.1:c.69554C>G (TTN)	XP_024308864.1:p.Pro23185Arg
XM_024453097.1:c.66896C>G (TTN)	XP_024308865.1:p.Pro22299Arg
XM_024453098.1:c.66815C>G (TTN)	XP_024308866.1:p.Pro22272Arg
XM_024453099.1:c.48578C>G (TTN)	XP_024308867.1:p.Pro16193Arg
XM_024453100.1:c.38432C>G (TTN)	XP_024308868.1:p.Pro12811Arg