Canonical Allele Identifier: CA349608961

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179480087A>C (hg19) ; chr2:g.178615360A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178615360A>C , CM000664.2:g.178615360A>C	GRCh38
NC_000002.11:g.179480087A>C , CM000664.1:g.179480087A>C	GRCh37
NC_000002.10:g.179188332A>C	NCBI36
NG_011618.3:g.220443T>G , LRG_391:g.220443T>G
NG_051363.1:g.97534A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.40881T>G (TTN)	ENSP00000343764.6:p.Cys13627Trp
ENST00000342175.11:c.21966T>G (TTN)	ENSP00000340554.6:p.Cys7322Trp
ENST00000359218.10:c.21765T>G (TTN)	ENSP00000352154.5:p.Cys7255Trp
ENST00000342175.10:c.21966T>G (TTN)	ENSP00000340554.6:p.Cys7322Trp
ENST00000342992.10:c.40881T>G (TTN)	ENSP00000343764.6:p.Cys13627Trp
ENST00000359218.9:c.21765T>G (TTN)	ENSP00000352154.5:p.Cys7255Trp
ENST00000460472.6:c.21390T>G (TTN)	ENSP00000434586.1:p.Cys7130Trp
ENST00000589042.5:c.48585T>G (TTN) MANE Select	ENSP00000467141.1:p.Cys16195Trp
ENST00000591111.5:c.43662T>G (TTN)	ENSP00000465570.1:p.Cys14554Trp
ENST00000615779.4:c.43662T>G (TTN)	ENSP00000483597.1:p.Cys14554Trp
NM_001256850.1:c.43662T>G (TTN)	NP_001243779.1:p.Cys14554Trp
NM_001267550.2:c.48585T>G (TTN) MANE Select	NP_001254479.2:p.Cys16195Trp
NM_003319.4:c.21390T>G (TTN)	NP_003310.4:p.Cys7130Trp
NM_133378.4:c.40881T>G (TTN)	NP_596869.4:p.Cys13627Trp
NM_133432.3:c.21765T>G (TTN)	NP_597676.3:p.Cys7255Trp
NM_133437.4:c.21966T>G (TTN)	NP_597681.4:p.Cys7322Trp
NR_038271.1:n.1590A>C (TTN-AS1)
XM_011511729.1:c.47682T>G (TTN)	XP_011510031.1:p.Cys15894Trp
XM_011511730.1:c.21576T>G (TTN)	XP_011510032.1:p.Cys7192Trp
XM_011511731.1:c.21435T>G (TTN)	XP_011510033.1:p.Cys7145Trp
XM_017004819.1:c.47478T>G (TTN)	XP_016860308.1:p.Cys15826Trp
XM_017004820.1:c.42876T>G (TTN)	XP_016860309.1:p.Cys14292Trp
XM_017004821.1:c.42873T>G (TTN)	XP_016860310.1:p.Cys14291Trp
XM_017004822.1:c.39915T>G (TTN)	XP_016860311.1:p.Cys13305Trp
XM_017004823.1:c.21531T>G (TTN)	XP_016860312.1:p.Cys7177Trp
XM_024453094.1:c.43026T>G (TTN)	XP_024308862.1:p.Cys14342Trp
XM_024453095.1:c.43023T>G (TTN)	XP_024308863.1:p.Cys14341Trp
XM_024453096.1:c.42456T>G (TTN)	XP_024308864.1:p.Cys14152Trp
XM_024453097.1:c.39798T>G (TTN)	XP_024308865.1:p.Cys13266Trp
XM_024453098.1:c.39717T>G (TTN)	XP_024308866.1:p.Cys13239Trp
XM_024453099.1:c.21480T>G (TTN)	XP_024308867.1:p.Cys7160Trp
XM_024453100.1:c.11334T>G (TTN)	XP_024308868.1:p.Cys3778Trp