Canonical Allele Identifier: CA430103975

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179416358T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178551631T>C , CM000664.2:g.178551631T>C	GRCh38
NC_000002.11:g.179416358T>C , CM000664.1:g.179416358T>C	GRCh37
NC_000002.10:g.179124604T>C	NCBI36
NG_011618.3:g.284172A>G , LRG_391:g.284172A>G
NG_051363.1:g.33805T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.83565A>G (TTN)	ENSP00000343764.6:p.Val27855=
ENST00000342175.11:c.64650A>G (TTN)	ENSP00000340554.6:p.Val21550=
ENST00000359218.10:c.64449A>G (TTN)	ENSP00000352154.5:p.Val21483=
ENST00000342175.10:c.64650A>G (TTN)	ENSP00000340554.6:p.Val21550=
ENST00000342992.10:c.83565A>G (TTN)	ENSP00000343764.6:p.Val27855=
ENST00000359218.9:c.64449A>G (TTN)	ENSP00000352154.5:p.Val21483=
ENST00000460472.6:c.64074A>G (TTN)	ENSP00000434586.1:p.Val21358=
ENST00000589042.5:c.91269A>G (TTN) MANE Select	ENSP00000467141.1:p.Val30423=
ENST00000591111.5:c.86346A>G (TTN)	ENSP00000465570.1:p.Val28782=
ENST00000615779.4:c.86346A>G (TTN)	ENSP00000483597.1:p.Val28782=
NM_001256850.1:c.86346A>G (TTN)	NP_001243779.1:p.Val28782=
NM_001267550.2:c.91269A>G (TTN) MANE Select	NP_001254479.2:p.Val30423=
NM_003319.4:c.64074A>G (TTN)	NP_003310.4:p.Val21358=
NM_133378.4:c.83565A>G (TTN)	NP_596869.4:p.Val27855=
NM_133432.3:c.64449A>G (TTN)	NP_597676.3:p.Val21483=
NM_133437.4:c.64650A>G (TTN)	NP_597681.4:p.Val21550=
NR_038271.1:n.447-19669T>C (TTN-AS1)
NR_038272.1:n.2043+9270T>C (TTN-AS1)
XM_011511729.1:c.90366A>G (TTN)	XP_011510031.1:p.Val30122=
XM_011511730.1:c.64260A>G (TTN)	XP_011510032.1:p.Val21420=
XM_011511731.1:c.64119A>G (TTN)	XP_011510033.1:p.Val21373=
XM_017004819.1:c.90162A>G (TTN)	XP_016860308.1:p.Val30054=
XM_017004820.1:c.85560A>G (TTN)	XP_016860309.1:p.Val28520=
XM_017004821.1:c.85557A>G (TTN)	XP_016860310.1:p.Val28519=
XM_017004822.1:c.82599A>G (TTN)	XP_016860311.1:p.Val27533=
XM_017004823.1:c.64215A>G (TTN)	XP_016860312.1:p.Val21405=
XM_024453094.1:c.85710A>G (TTN)	XP_024308862.1:p.Val28570=
XM_024453095.1:c.85707A>G (TTN)	XP_024308863.1:p.Val28569=
XM_024453096.1:c.85140A>G (TTN)	XP_024308864.1:p.Val28380=
XM_024453097.1:c.82482A>G (TTN)	XP_024308865.1:p.Val27494=
XM_024453098.1:c.82401A>G (TTN)	XP_024308866.1:p.Val27467=
XM_024453099.1:c.64164A>G (TTN)	XP_024308867.1:p.Val21388=
XM_024453100.1:c.54018A>G (TTN)	XP_024308868.1:p.Val18006=