Canonical Allele Identifier: CA349636178

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178572134A>T , CM000664.2:g.178572134A>T	GRCh38
NC_000002.11:g.179436861A>T , CM000664.1:g.179436861A>T	GRCh37
NC_000002.10:g.179145107A>T	NCBI36
NG_011618.3:g.263669T>A , LRG_391:g.263669T>A
NG_051363.1:g.54308A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.73998T>A (TTN) MANE Select	NP_001254479.2:p.Cys24666Ter
ENST00000589042.5:c.73998T>A (TTN) MANE Select	ENSP00000467141.1:p.Cys24666Ter
NM_001256850.1:c.69075T>A (TTN)	NP_001243779.1:p.Cys23025Ter
NM_003319.4:c.46803T>A (TTN)	NP_003310.4:p.Cys15601Ter
NM_133378.4:c.66294T>A (TTN)	NP_596869.4:p.Cys22098Ter
NM_133432.3:c.47178T>A (TTN)	NP_597676.3:p.Cys15726Ter
NM_133437.4:c.47379T>A (TTN)	NP_597681.4:p.Cys15793Ter
NR_038271.1:n.596+685A>T (TTN-AS1)
NR_038272.1:n.2044-10438A>T (TTN-AS1)
ENST00000342175.10:c.47379T>A (TTN)	ENSP00000340554.6:p.Cys15793Ter
ENST00000342175.11:c.47379T>A (TTN)	ENSP00000340554.6:p.Cys15793Ter
ENST00000342992.10:c.66294T>A (TTN)	ENSP00000343764.6:p.Cys22098Ter
ENST00000342992.11:c.66294T>A (TTN)	ENSP00000343764.6:p.Cys22098Ter
ENST00000359218.10:c.47178T>A (TTN)	ENSP00000352154.5:p.Cys15726Ter
ENST00000359218.9:c.47178T>A (TTN)	ENSP00000352154.5:p.Cys15726Ter
ENST00000460472.6:c.46803T>A (TTN)	ENSP00000434586.1:p.Cys15601Ter
ENST00000591111.5:c.69075T>A (TTN)	ENSP00000465570.1:p.Cys23025Ter
ENST00000615779.4:c.69075T>A (TTN)	ENSP00000483597.1:p.Cys23025Ter
XM_011511729.1:c.73095T>A (TTN)	XP_011510031.1:p.Cys24365Ter
XM_011511730.1:c.46989T>A (TTN)	XP_011510032.1:p.Cys15663Ter
XM_011511731.1:c.46848T>A (TTN)	XP_011510033.1:p.Cys15616Ter
XM_017004819.1:c.72891T>A (TTN)	XP_016860308.1:p.Cys24297Ter
XM_017004820.1:c.68289T>A (TTN)	XP_016860309.1:p.Cys22763Ter
XM_017004821.1:c.68286T>A (TTN)	XP_016860310.1:p.Cys22762Ter
XM_017004822.1:c.65328T>A (TTN)	XP_016860311.1:p.Cys21776Ter
XM_017004823.1:c.46944T>A (TTN)	XP_016860312.1:p.Cys15648Ter
XM_024453094.1:c.68439T>A (TTN)	XP_024308862.1:p.Cys22813Ter
XM_024453095.1:c.68436T>A (TTN)	XP_024308863.1:p.Cys22812Ter
XM_024453096.1:c.67869T>A (TTN)	XP_024308864.1:p.Cys22623Ter
XM_024453097.1:c.65211T>A (TTN)	XP_024308865.1:p.Cys21737Ter
XM_024453098.1:c.65130T>A (TTN)	XP_024308866.1:p.Cys21710Ter
XM_024453099.1:c.46893T>A (TTN)	XP_024308867.1:p.Cys15631Ter
XM_024453100.1:c.36747T>A (TTN)	XP_024308868.1:p.Cys12249Ter