Canonical Allele Identifier: CA349456911

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179409110T>G (hg19) ; chr2:g.178544383T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178544383T>G , CM000664.2:g.178544383T>G	GRCh38
NC_000002.11:g.179409110T>G , CM000664.1:g.179409110T>G	GRCh37
NC_000002.10:g.179117356T>G	NCBI36
NG_011618.3:g.291420A>C , LRG_391:g.291420A>C
NG_051363.1:g.26557T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.88142A>C (TTN)	ENSP00000343764.6:p.Gln29381Pro
ENST00000342175.11:c.69227A>C (TTN)	ENSP00000340554.6:p.Gln23076Pro
ENST00000359218.10:c.69026A>C (TTN)	ENSP00000352154.5:p.Gln23009Pro
ENST00000342175.10:c.69227A>C (TTN)	ENSP00000340554.6:p.Gln23076Pro
ENST00000342992.10:c.88142A>C (TTN)	ENSP00000343764.6:p.Gln29381Pro
ENST00000359218.9:c.69026A>C (TTN)	ENSP00000352154.5:p.Gln23009Pro
ENST00000460472.6:c.68651A>C (TTN)	ENSP00000434586.1:p.Gln22884Pro
ENST00000589042.5:c.95846A>C (TTN) MANE Select	ENSP00000467141.1:p.Gln31949Pro
ENST00000591111.5:c.90923A>C (TTN)	ENSP00000465570.1:p.Gln30308Pro
ENST00000615779.4:c.90923A>C (TTN)	ENSP00000483597.1:p.Gln30308Pro
NM_001256850.1:c.90923A>C (TTN)	NP_001243779.1:p.Gln30308Pro
NM_001267550.2:c.95846A>C (TTN) MANE Select	NP_001254479.2:p.Gln31949Pro
NM_003319.4:c.68651A>C (TTN)	NP_003310.4:p.Gln22884Pro
NM_133378.4:c.88142A>C (TTN)	NP_596869.4:p.Gln29381Pro
NM_133432.3:c.69026A>C (TTN)	NP_597676.3:p.Gln23009Pro
NM_133437.4:c.69227A>C (TTN)	NP_597681.4:p.Gln23076Pro
NR_038271.1:n.446+20747T>G (TTN-AS1)
NR_038272.1:n.2043+2022T>G (TTN-AS1)
XM_011511729.1:c.94943A>C (TTN)	XP_011510031.1:p.Gln31648Pro
XM_011511730.1:c.68837A>C (TTN)	XP_011510032.1:p.Gln22946Pro
XM_011511731.1:c.68696A>C (TTN)	XP_011510033.1:p.Gln22899Pro
XM_017004819.1:c.94739A>C (TTN)	XP_016860308.1:p.Gln31580Pro
XM_017004820.1:c.90137A>C (TTN)	XP_016860309.1:p.Gln30046Pro
XM_017004821.1:c.90134A>C (TTN)	XP_016860310.1:p.Gln30045Pro
XM_017004822.1:c.87176A>C (TTN)	XP_016860311.1:p.Gln29059Pro
XM_017004823.1:c.68792A>C (TTN)	XP_016860312.1:p.Gln22931Pro
XM_024453094.1:c.90287A>C (TTN)	XP_024308862.1:p.Gln30096Pro
XM_024453095.1:c.90284A>C (TTN)	XP_024308863.1:p.Gln30095Pro
XM_024453096.1:c.89717A>C (TTN)	XP_024308864.1:p.Gln29906Pro
XM_024453097.1:c.87059A>C (TTN)	XP_024308865.1:p.Gln29020Pro
XM_024453098.1:c.86978A>C (TTN)	XP_024308866.1:p.Gln28993Pro
XM_024453099.1:c.68741A>C (TTN)	XP_024308867.1:p.Gln22914Pro
XM_024453100.1:c.58595A>C (TTN)	XP_024308868.1:p.Gln19532Pro