Canonical Allele Identifier: CA349483597

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179455844G>C (hg19) ; chr2:g.178591117G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178591117G>C , CM000664.2:g.178591117G>C	GRCh38
NC_000002.11:g.179455844G>C , CM000664.1:g.179455844G>C	GRCh37
NC_000002.10:g.179164090G>C	NCBI36
NG_011618.3:g.244686C>G , LRG_391:g.244686C>G
NG_051363.1:g.73291G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.52904C>G (TTN)	ENSP00000343764.6:p.Pro17635Arg
ENST00000342175.11:c.33989C>G (TTN)	ENSP00000340554.6:p.Pro11330Arg
ENST00000359218.10:c.33788C>G (TTN)	ENSP00000352154.5:p.Pro11263Arg
ENST00000342175.10:c.33989C>G (TTN)	ENSP00000340554.6:p.Pro11330Arg
ENST00000342992.10:c.52904C>G (TTN)	ENSP00000343764.6:p.Pro17635Arg
ENST00000359218.9:c.33788C>G (TTN)	ENSP00000352154.5:p.Pro11263Arg
ENST00000460472.6:c.33413C>G (TTN)	ENSP00000434586.1:p.Pro11138Arg
ENST00000589042.5:c.60608C>G (TTN) MANE Select	ENSP00000467141.1:p.Pro20203Arg
ENST00000591111.5:c.55685C>G (TTN)	ENSP00000465570.1:p.Pro18562Arg
ENST00000615779.4:c.55685C>G (TTN)	ENSP00000483597.1:p.Pro18562Arg
NM_001256850.1:c.55685C>G (TTN)	NP_001243779.1:p.Pro18562Arg
NM_001267550.2:c.60608C>G (TTN) MANE Select	NP_001254479.2:p.Pro20203Arg
NM_003319.4:c.33413C>G (TTN)	NP_003310.4:p.Pro11138Arg
NM_133378.4:c.52904C>G (TTN)	NP_596869.4:p.Pro17635Arg
NM_133432.3:c.33788C>G (TTN)	NP_597676.3:p.Pro11263Arg
NM_133437.4:c.33989C>G (TTN)	NP_597681.4:p.Pro11330Arg
NR_038271.1:n.597-6479G>C (TTN-AS1)
NR_038272.1:n.3189-22G>C (TTN-AS1)
XM_011511729.1:c.59705C>G (TTN)	XP_011510031.1:p.Pro19902Arg
XM_011511730.1:c.33599C>G (TTN)	XP_011510032.1:p.Pro11200Arg
XM_011511731.1:c.33458C>G (TTN)	XP_011510033.1:p.Pro11153Arg
XM_017004819.1:c.59501C>G (TTN)	XP_016860308.1:p.Pro19834Arg
XM_017004820.1:c.54899C>G (TTN)	XP_016860309.1:p.Pro18300Arg
XM_017004821.1:c.54896C>G (TTN)	XP_016860310.1:p.Pro18299Arg
XM_017004822.1:c.51938C>G (TTN)	XP_016860311.1:p.Pro17313Arg
XM_017004823.1:c.33554C>G (TTN)	XP_016860312.1:p.Pro11185Arg
XM_024453094.1:c.55049C>G (TTN)	XP_024308862.1:p.Pro18350Arg
XM_024453095.1:c.55046C>G (TTN)	XP_024308863.1:p.Pro18349Arg
XM_024453096.1:c.54479C>G (TTN)	XP_024308864.1:p.Pro18160Arg
XM_024453097.1:c.51821C>G (TTN)	XP_024308865.1:p.Pro17274Arg
XM_024453098.1:c.51740C>G (TTN)	XP_024308866.1:p.Pro17247Arg
XM_024453099.1:c.33503C>G (TTN)	XP_024308867.1:p.Pro11168Arg
XM_024453100.1:c.23357C>G (TTN)	XP_024308868.1:p.Pro7786Arg