Canonical Allele Identifier: CA430277648

Gene: TTN

Linked Data

• MyVariant Identifiers: chr2:g.179500168T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178635441T>G , CM000664.2:g.178635441T>G	GRCh38
NC_000002.11:g.179500168T>G , CM000664.1:g.179500168T>G	GRCh37
NC_000002.10:g.179208413T>G	NCBI36
NG_011618.3:g.200362A>C , LRG_391:g.200362A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.34179A>C	ENSP00000343764.6:p.Gly11393=
ENST00000342175.11:c.15264A>C	ENSP00000340554.6:p.Gly5088=
ENST00000359218.10:c.15063A>C	ENSP00000352154.5:p.Gly5021=
ENST00000342175.10:c.15264A>C	ENSP00000340554.6:p.Gly5088=
ENST00000342992.10:c.34179A>C	ENSP00000343764.6:p.Gly11393=
ENST00000359218.9:c.15063A>C	ENSP00000352154.5:p.Gly5021=
ENST00000460472.6:c.14688A>C	ENSP00000434586.1:p.Gly4896=
ENST00000589042.5:c.41883A>C MANE Select	ENSP00000467141.1:p.Gly13961=
ENST00000591111.5:c.36960A>C	ENSP00000465570.1:p.Gly12320=
ENST00000615779.4:c.36960A>C	ENSP00000483597.1:p.Gly12320=
NM_001256850.1:c.36960A>C	NP_001243779.1:p.Gly12320=
NM_001267550.2:c.41883A>C MANE Select	NP_001254479.2:p.Gly13961=
NM_003319.4:c.14688A>C	NP_003310.4:p.Gly4896=
NM_133378.4:c.34179A>C	NP_596869.4:p.Gly11393=
NM_133432.3:c.15063A>C	NP_597676.3:p.Gly5021=
NM_133437.4:c.15264A>C	NP_597681.4:p.Gly5088=
XM_011511729.1:c.40980A>C	XP_011510031.1:p.Gly13660=
XM_011511730.1:c.14874A>C	XP_011510032.1:p.Gly4958=
XM_011511731.1:c.14733A>C	XP_011510033.1:p.Gly4911=
XM_017004819.1:c.40776A>C	XP_016860308.1:p.Gly13592=
XM_017004820.1:c.36174A>C	XP_016860309.1:p.Gly12058=
XM_017004821.1:c.36171A>C	XP_016860310.1:p.Gly12057=
XM_017004822.1:c.33213A>C	XP_016860311.1:p.Gly11071=
XM_017004823.1:c.14829A>C	XP_016860312.1:p.Gly4943=
XM_024453094.1:c.36324A>C	XP_024308862.1:p.Gly12108=
XM_024453095.1:c.36321A>C	XP_024308863.1:p.Gly12107=
XM_024453096.1:c.35754A>C	XP_024308864.1:p.Gly11918=
XM_024453097.1:c.33096A>C	XP_024308865.1:p.Gly11032=
XM_024453098.1:c.33015A>C	XP_024308866.1:p.Gly11005=
XM_024453099.1:c.14778A>C	XP_024308867.1:p.Gly4926=
XM_024453100.1:c.4632A>C	XP_024308868.1:p.Gly1544=