Canonical Allele Identifier: CA349507112

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179458753T>G (hg19) ; chr2:g.178594026T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178594026T>G , CM000664.2:g.178594026T>G	GRCh38
NC_000002.11:g.179458753T>G , CM000664.1:g.179458753T>G	GRCh37
NC_000002.10:g.179166999T>G	NCBI36
NG_011618.3:g.241777A>C , LRG_391:g.241777A>C
NG_051363.1:g.76200T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.50663A>C (TTN)	ENSP00000343764.6:p.Lys16888Thr
ENST00000342175.11:c.31748A>C (TTN)	ENSP00000340554.6:p.Lys10583Thr
ENST00000359218.10:c.31547A>C (TTN)	ENSP00000352154.5:p.Lys10516Thr
ENST00000342175.10:c.31748A>C (TTN)	ENSP00000340554.6:p.Lys10583Thr
ENST00000342992.10:c.50663A>C (TTN)	ENSP00000343764.6:p.Lys16888Thr
ENST00000359218.9:c.31547A>C (TTN)	ENSP00000352154.5:p.Lys10516Thr
ENST00000460472.6:c.31172A>C (TTN)	ENSP00000434586.1:p.Lys10391Thr
ENST00000589042.5:c.58367A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys19456Thr
ENST00000591111.5:c.53444A>C (TTN)	ENSP00000465570.1:p.Lys17815Thr
ENST00000615779.4:c.53444A>C (TTN)	ENSP00000483597.1:p.Lys17815Thr
NM_001256850.1:c.53444A>C (TTN)	NP_001243779.1:p.Lys17815Thr
NM_001267550.2:c.58367A>C (TTN) MANE Select	NP_001254479.2:p.Lys19456Thr
NM_003319.4:c.31172A>C (TTN)	NP_003310.4:p.Lys10391Thr
NM_133378.4:c.50663A>C (TTN)	NP_596869.4:p.Lys16888Thr
NM_133432.3:c.31547A>C (TTN)	NP_597676.3:p.Lys10516Thr
NM_133437.4:c.31748A>C (TTN)	NP_597681.4:p.Lys10583Thr
NR_038271.1:n.597-3570T>G (TTN-AS1)
NR_038272.1:n.3364+2712T>G (TTN-AS1)
XM_011511729.1:c.57464A>C (TTN)	XP_011510031.1:p.Lys19155Thr
XM_011511730.1:c.31358A>C (TTN)	XP_011510032.1:p.Lys10453Thr
XM_011511731.1:c.31217A>C (TTN)	XP_011510033.1:p.Lys10406Thr
XM_017004819.1:c.57260A>C (TTN)	XP_016860308.1:p.Lys19087Thr
XM_017004820.1:c.52658A>C (TTN)	XP_016860309.1:p.Lys17553Thr
XM_017004821.1:c.52655A>C (TTN)	XP_016860310.1:p.Lys17552Thr
XM_017004822.1:c.49697A>C (TTN)	XP_016860311.1:p.Lys16566Thr
XM_017004823.1:c.31313A>C (TTN)	XP_016860312.1:p.Lys10438Thr
XM_024453094.1:c.52808A>C (TTN)	XP_024308862.1:p.Lys17603Thr
XM_024453095.1:c.52805A>C (TTN)	XP_024308863.1:p.Lys17602Thr
XM_024453096.1:c.52238A>C (TTN)	XP_024308864.1:p.Lys17413Thr
XM_024453097.1:c.49580A>C (TTN)	XP_024308865.1:p.Lys16527Thr
XM_024453098.1:c.49499A>C (TTN)	XP_024308866.1:p.Lys16500Thr
XM_024453099.1:c.31262A>C (TTN)	XP_024308867.1:p.Lys10421Thr
XM_024453100.1:c.21116A>C (TTN)	XP_024308868.1:p.Lys7039Thr