Canonical Allele Identifier: CA1310535813

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178581650G= , CM000664.2:g.178581650G=	GRCh38
NC_000002.11:g.179446377G= , CM000664.1:g.179446377G=	GRCh37
NC_000002.10:g.179154623G=	NCBI36
NG_011618.3:g.254153C= , LRG_391:g.254153C=
NG_051363.1:g.63824G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.66618C= (TTN) MANE Select	NP_001254479.2:p.Cys22206=
ENST00000589042.5:c.66618C= (TTN) MANE Select	ENSP00000467141.1:p.Cys22206=
NM_001256850.1:c.61695C= (TTN)	NP_001243779.1:p.Cys20565=
NM_003319.4:c.39423C= (TTN)	NP_003310.4:p.Cys13141=
NM_133378.4:c.58914C= (TTN)	NP_596869.4:p.Cys19638=
NM_133432.3:c.39798C= (TTN)	NP_597676.3:p.Cys13266=
NM_133437.4:c.39999C= (TTN)	NP_597681.4:p.Cys13333=
NR_038271.1:n.596+10201G= (TTN-AS1)
NR_038272.1:n.2044-922G= (TTN-AS1)
ENST00000342175.10:c.39999C= (TTN)	ENSP00000340554.6:p.Cys13333=
ENST00000342175.11:c.39999C= (TTN)	ENSP00000340554.6:p.Cys13333=
ENST00000342992.10:c.58914C= (TTN)	ENSP00000343764.6:p.Cys19638=
ENST00000342992.11:c.58914C= (TTN)	ENSP00000343764.6:p.Cys19638=
ENST00000359218.10:c.39798C= (TTN)	ENSP00000352154.5:p.Cys13266=
ENST00000359218.9:c.39798C= (TTN)	ENSP00000352154.5:p.Cys13266=
ENST00000460472.6:c.39423C= (TTN)	ENSP00000434586.1:p.Cys13141=
ENST00000591111.5:c.61695C= (TTN)	ENSP00000465570.1:p.Cys20565=
ENST00000615779.4:c.61695C= (TTN)	ENSP00000483597.1:p.Cys20565=
XM_011511729.1:c.65715C= (TTN)	XP_011510031.1:p.Cys21905=
XM_011511730.1:c.39609C= (TTN)	XP_011510032.1:p.Cys13203=
XM_011511731.1:c.39468C= (TTN)	XP_011510033.1:p.Cys13156=
XM_017004819.1:c.65511C= (TTN)	XP_016860308.1:p.Cys21837=
XM_017004820.1:c.60909C= (TTN)	XP_016860309.1:p.Cys20303=
XM_017004821.1:c.60906C= (TTN)	XP_016860310.1:p.Cys20302=
XM_017004822.1:c.57948C= (TTN)	XP_016860311.1:p.Cys19316=
XM_017004823.1:c.39564C= (TTN)	XP_016860312.1:p.Cys13188=
XM_024453094.1:c.61059C= (TTN)	XP_024308862.1:p.Cys20353=
XM_024453095.1:c.61056C= (TTN)	XP_024308863.1:p.Cys20352=
XM_024453096.1:c.60489C= (TTN)	XP_024308864.1:p.Cys20163=
XM_024453097.1:c.57831C= (TTN)	XP_024308865.1:p.Cys19277=
XM_024453098.1:c.57750C= (TTN)	XP_024308866.1:p.Cys19250=
XM_024453099.1:c.39513C= (TTN)	XP_024308867.1:p.Cys13171=
XM_024453100.1:c.29367C= (TTN)	XP_024308868.1:p.Cys9789=