Canonical Allele Identifier: CA349422863

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179400525T>C (hg19) ; chr2:g.178535798T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178535798T>C , CM000664.2:g.178535798T>C	GRCh38
NC_000002.11:g.179400525T>C , CM000664.1:g.179400525T>C	GRCh37
NC_000002.10:g.179108771T>C	NCBI36
NG_011618.3:g.300005A>G , LRG_391:g.300005A>G
NG_051363.1:g.17972T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.93113A>G (TTN)	ENSP00000343764.6:p.His31038Arg
ENST00000342175.11:c.74198A>G (TTN)	ENSP00000340554.6:p.His24733Arg
ENST00000359218.10:c.73997A>G (TTN)	ENSP00000352154.5:p.His24666Arg
ENST00000342175.10:c.74198A>G (TTN)	ENSP00000340554.6:p.His24733Arg
ENST00000342992.10:c.93113A>G (TTN)	ENSP00000343764.6:p.His31038Arg
ENST00000359218.9:c.73997A>G (TTN)	ENSP00000352154.5:p.His24666Arg
ENST00000460472.6:c.73622A>G (TTN)	ENSP00000434586.1:p.His24541Arg
ENST00000589042.5:c.100817A>G (TTN) MANE Select	ENSP00000467141.1:p.His33606Arg
ENST00000591111.5:c.95894A>G (TTN)	ENSP00000465570.1:p.His31965Arg
ENST00000615779.4:c.95894A>G (TTN)	ENSP00000483597.1:p.His31965Arg
NM_001256850.1:c.95894A>G (TTN)	NP_001243779.1:p.His31965Arg
NM_001267550.2:c.100817A>G (TTN) MANE Select	NP_001254479.2:p.His33606Arg
NM_003319.4:c.73622A>G (TTN)	NP_003310.4:p.His24541Arg
NM_133378.4:c.93113A>G (TTN)	NP_596869.4:p.His31038Arg
NM_133432.3:c.73997A>G (TTN)	NP_597676.3:p.His24666Arg
NM_133437.4:c.74198A>G (TTN)	NP_597681.4:p.His24733Arg
NR_038271.1:n.446+12162T>C (TTN-AS1)
NR_038272.1:n.286T>C (TTN-AS1)
XM_011511729.1:c.99914A>G (TTN)	XP_011510031.1:p.His33305Arg
XM_011511730.1:c.73808A>G (TTN)	XP_011510032.1:p.His24603Arg
XM_011511731.1:c.73667A>G (TTN)	XP_011510033.1:p.His24556Arg
XM_017004819.1:c.99710A>G (TTN)	XP_016860308.1:p.His33237Arg
XM_017004820.1:c.95108A>G (TTN)	XP_016860309.1:p.His31703Arg
XM_017004821.1:c.95105A>G (TTN)	XP_016860310.1:p.His31702Arg
XM_017004822.1:c.92147A>G (TTN)	XP_016860311.1:p.His30716Arg
XM_017004823.1:c.73763A>G (TTN)	XP_016860312.1:p.His24588Arg
XM_024453094.1:c.95258A>G (TTN)	XP_024308862.1:p.His31753Arg
XM_024453095.1:c.95255A>G (TTN)	XP_024308863.1:p.His31752Arg
XM_024453096.1:c.94688A>G (TTN)	XP_024308864.1:p.His31563Arg
XM_024453097.1:c.92030A>G (TTN)	XP_024308865.1:p.His30677Arg
XM_024453098.1:c.91949A>G (TTN)	XP_024308866.1:p.His30650Arg
XM_024453099.1:c.73712A>G (TTN)	XP_024308867.1:p.His24571Arg
XM_024453100.1:c.63566A>G (TTN)	XP_024308868.1:p.His21189Arg