Canonical Allele Identifier: CA349573256

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179428370C>G (hg19) ; chr2:g.178563643C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178563643C>G , CM000664.2:g.178563643C>G	GRCh38
NC_000002.11:g.179428370C>G , CM000664.1:g.179428370C>G	GRCh37
NC_000002.10:g.179136616C>G	NCBI36
NG_011618.3:g.272160G>C , LRG_391:g.272160G>C
NG_051363.1:g.45817C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.74785G>C (TTN)	ENSP00000343764.6:p.Gly24929Arg
ENST00000342175.11:c.55870G>C (TTN)	ENSP00000340554.6:p.Gly18624Arg
ENST00000359218.10:c.55669G>C (TTN)	ENSP00000352154.5:p.Gly18557Arg
ENST00000342175.10:c.55870G>C (TTN)	ENSP00000340554.6:p.Gly18624Arg
ENST00000342992.10:c.74785G>C (TTN)	ENSP00000343764.6:p.Gly24929Arg
ENST00000359218.9:c.55669G>C (TTN)	ENSP00000352154.5:p.Gly18557Arg
ENST00000460472.6:c.55294G>C (TTN)	ENSP00000434586.1:p.Gly18432Arg
ENST00000589042.5:c.82489G>C (TTN) MANE Select	ENSP00000467141.1:p.Gly27497Arg
ENST00000591111.5:c.77566G>C (TTN)	ENSP00000465570.1:p.Gly25856Arg
ENST00000615779.4:c.77566G>C (TTN)	ENSP00000483597.1:p.Gly25856Arg
NM_001256850.1:c.77566G>C (TTN)	NP_001243779.1:p.Gly25856Arg
NM_001267550.2:c.82489G>C (TTN) MANE Select	NP_001254479.2:p.Gly27497Arg
NM_003319.4:c.55294G>C (TTN)	NP_003310.4:p.Gly18432Arg
NM_133378.4:c.74785G>C (TTN)	NP_596869.4:p.Gly24929Arg
NM_133432.3:c.55669G>C (TTN)	NP_597676.3:p.Gly18557Arg
NM_133437.4:c.55870G>C (TTN)	NP_597681.4:p.Gly18624Arg
NR_038271.1:n.447-7657C>G (TTN-AS1)
NR_038272.1:n.2044-18929C>G (TTN-AS1)
XM_011511729.1:c.81586G>C (TTN)	XP_011510031.1:p.Gly27196Arg
XM_011511730.1:c.55480G>C (TTN)	XP_011510032.1:p.Gly18494Arg
XM_011511731.1:c.55339G>C (TTN)	XP_011510033.1:p.Gly18447Arg
XM_017004819.1:c.81382G>C (TTN)	XP_016860308.1:p.Gly27128Arg
XM_017004820.1:c.76780G>C (TTN)	XP_016860309.1:p.Gly25594Arg
XM_017004821.1:c.76777G>C (TTN)	XP_016860310.1:p.Gly25593Arg
XM_017004822.1:c.73819G>C (TTN)	XP_016860311.1:p.Gly24607Arg
XM_017004823.1:c.55435G>C (TTN)	XP_016860312.1:p.Gly18479Arg
XM_024453094.1:c.76930G>C (TTN)	XP_024308862.1:p.Gly25644Arg
XM_024453095.1:c.76927G>C (TTN)	XP_024308863.1:p.Gly25643Arg
XM_024453096.1:c.76360G>C (TTN)	XP_024308864.1:p.Gly25454Arg
XM_024453097.1:c.73702G>C (TTN)	XP_024308865.1:p.Gly24568Arg
XM_024453098.1:c.73621G>C (TTN)	XP_024308866.1:p.Gly24541Arg
XM_024453099.1:c.55384G>C (TTN)	XP_024308867.1:p.Gly18462Arg
XM_024453100.1:c.45238G>C (TTN)	XP_024308868.1:p.Gly15080Arg