Canonical Allele Identifier: CA349411903

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396979C>G (hg19) ; chr2:g.178532252C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178532252C>G , CM000664.2:g.178532252C>G	GRCh38
NC_000002.11:g.179396979C>G , CM000664.1:g.179396979C>G	GRCh37
NC_000002.10:g.179105225C>G	NCBI36
NG_011618.3:g.303551G>C , LRG_391:g.303551G>C
NG_051363.1:g.14426C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.96659G>C (TTN)	ENSP00000343764.6:p.Ser32220Thr
ENST00000342175.11:c.77744G>C (TTN)	ENSP00000340554.6:p.Ser25915Thr
ENST00000359218.10:c.77543G>C (TTN)	ENSP00000352154.5:p.Ser25848Thr
ENST00000342175.10:c.77744G>C (TTN)	ENSP00000340554.6:p.Ser25915Thr
ENST00000342992.10:c.96659G>C (TTN)	ENSP00000343764.6:p.Ser32220Thr
ENST00000359218.9:c.77543G>C (TTN)	ENSP00000352154.5:p.Ser25848Thr
ENST00000460472.6:c.77168G>C (TTN)	ENSP00000434586.1:p.Ser25723Thr
ENST00000589042.5:c.104363G>C (TTN) MANE Select	ENSP00000467141.1:p.Ser34788Thr
ENST00000591111.5:c.99440G>C (TTN)	ENSP00000465570.1:p.Ser33147Thr
ENST00000615779.4:c.99440G>C (TTN)	ENSP00000483597.1:p.Ser33147Thr
NM_001256850.1:c.99440G>C (TTN)	NP_001243779.1:p.Ser33147Thr
NM_001267550.2:c.104363G>C (TTN) MANE Select	NP_001254479.2:p.Ser34788Thr
NM_003319.4:c.77168G>C (TTN)	NP_003310.4:p.Ser25723Thr
NM_133378.4:c.96659G>C (TTN)	NP_596869.4:p.Ser32220Thr
NM_133432.3:c.77543G>C (TTN)	NP_597676.3:p.Ser25848Thr
NM_133437.4:c.77744G>C (TTN)	NP_597681.4:p.Ser25915Thr
NR_038271.1:n.446+8616C>G (TTN-AS1)
NR_038272.1:n.220-3480C>G (TTN-AS1)
XM_011511729.1:c.103460G>C (TTN)	XP_011510031.1:p.Ser34487Thr
XM_011511730.1:c.77354G>C (TTN)	XP_011510032.1:p.Ser25785Thr
XM_011511731.1:c.77213G>C (TTN)	XP_011510033.1:p.Ser25738Thr
XM_017004819.1:c.103256G>C (TTN)	XP_016860308.1:p.Ser34419Thr
XM_017004820.1:c.98654G>C (TTN)	XP_016860309.1:p.Ser32885Thr
XM_017004821.1:c.98651G>C (TTN)	XP_016860310.1:p.Ser32884Thr
XM_017004822.1:c.95693G>C (TTN)	XP_016860311.1:p.Ser31898Thr
XM_017004823.1:c.77309G>C (TTN)	XP_016860312.1:p.Ser25770Thr
XM_024453094.1:c.98804G>C (TTN)	XP_024308862.1:p.Ser32935Thr
XM_024453095.1:c.98801G>C (TTN)	XP_024308863.1:p.Ser32934Thr
XM_024453096.1:c.98234G>C (TTN)	XP_024308864.1:p.Ser32745Thr
XM_024453097.1:c.95576G>C (TTN)	XP_024308865.1:p.Ser31859Thr
XM_024453098.1:c.95495G>C (TTN)	XP_024308866.1:p.Ser31832Thr
XM_024453099.1:c.77258G>C (TTN)	XP_024308867.1:p.Ser25753Thr
XM_024453100.1:c.67112G>C (TTN)	XP_024308868.1:p.Ser22371Thr