Canonical Allele Identifier: CA60988036

Gene: TTN TTN-AS1

Linked Data

• dbSNP Id: rs969149065
• MyVariant Identifiers: chr2:g.179480011C>G (hg19) ; chr2:g.178615284C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178615284C>G , CM000664.2:g.178615284C>G	GRCh38
NC_000002.11:g.179480011C>G , CM000664.1:g.179480011C>G	GRCh37
NC_000002.10:g.179188256C>G	NCBI36
NG_011618.3:g.220519G>C , LRG_391:g.220519G>C
NG_051363.1:g.97458C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.40934+23G>C (TTN)	ENSP00000343764.6:n.40934+23G>C
ENST00000342175.11:c.22019+23G>C (TTN)	ENSP00000340554.6:n.22019+23G>C
ENST00000359218.10:c.21818+23G>C (TTN)	ENSP00000352154.5:n.21818+23G>C
ENST00000342175.10:c.22019+23G>C (TTN)	ENSP00000340554.6:n.22019+23G>C
ENST00000342992.10:c.40934+23G>C (TTN)	ENSP00000343764.6:n.40934+23G>C
ENST00000359218.9:c.21818+23G>C (TTN)	ENSP00000352154.5:n.21818+23G>C
ENST00000460472.6:c.21443+23G>C (TTN)	ENSP00000434586.1:n.21443+23G>C
ENST00000589042.5:c.48638+23G>C (TTN) MANE Select	ENSP00000467141.1:n.48638+23G>C
ENST00000591111.5:c.43715+23G>C (TTN)	ENSP00000465570.1:n.43715+23G>C
ENST00000615779.4:c.43715+23G>C (TTN)	ENSP00000483597.1:n.43715+23G>C
NM_001256850.1:c.43715+23G>C (TTN)	NP_001243779.1:n.43715+23G>C
NM_001267550.2:c.48638+23G>C (TTN) MANE Select	NP_001254479.2:n.48638+23G>C
NM_003319.4:c.21443+23G>C (TTN)	NP_003310.4:n.21443+23G>C
NM_133378.4:c.40934+23G>C (TTN)	NP_596869.4:n.40934+23G>C
NM_133432.3:c.21818+23G>C (TTN)	NP_597676.3:n.21818+23G>C
NM_133437.4:c.22019+23G>C (TTN)	NP_597681.4:n.22019+23G>C
NR_038271.1:n.1553-39C>G (TTN-AS1)
XM_011511729.1:c.47735+23G>C (TTN)	XP_011510031.1:n.47735+23G>C
XM_011511730.1:c.21629+23G>C (TTN)	XP_011510032.1:n.21629+23G>C
XM_011511731.1:c.21488+23G>C (TTN)	XP_011510033.1:n.21488+23G>C
XM_017004819.1:c.47531+23G>C (TTN)	XP_016860308.1:n.47531+23G>C
XM_017004820.1:c.42929+23G>C (TTN)	XP_016860309.1:n.42929+23G>C
XM_017004821.1:c.42926+23G>C (TTN)	XP_016860310.1:n.42926+23G>C
XM_017004822.1:c.39968+23G>C (TTN)	XP_016860311.1:n.39968+23G>C
XM_017004823.1:c.21584+23G>C (TTN)	XP_016860312.1:n.21584+23G>C
XM_024453094.1:c.43079+23G>C (TTN)	XP_024308862.1:n.43079+23G>C
XM_024453095.1:c.43076+23G>C (TTN)	XP_024308863.1:n.43076+23G>C
XM_024453096.1:c.42509+23G>C (TTN)	XP_024308864.1:n.42509+23G>C
XM_024453097.1:c.39851+23G>C (TTN)	XP_024308865.1:n.39851+23G>C
XM_024453098.1:c.39770+23G>C (TTN)	XP_024308866.1:n.39770+23G>C
XM_024453099.1:c.21533+23G>C (TTN)	XP_024308867.1:n.21533+23G>C
XM_024453100.1:c.11387+23G>C (TTN)	XP_024308868.1:n.11387+23G>C