Canonical Allele Identifier: CA349600915

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179432020T>C (hg19) ; chr2:g.178567293T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178567293T>C , CM000664.2:g.178567293T>C	GRCh38
NC_000002.11:g.179432020T>C , CM000664.1:g.179432020T>C	GRCh37
NC_000002.10:g.179140266T>C	NCBI36
NG_011618.3:g.268510A>G , LRG_391:g.268510A>G
NG_051363.1:g.49467T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.71135A>G (TTN)	ENSP00000343764.6:p.Asn23712Ser
ENST00000342175.11:c.52220A>G (TTN)	ENSP00000340554.6:p.Asn17407Ser
ENST00000359218.10:c.52019A>G (TTN)	ENSP00000352154.5:p.Asn17340Ser
ENST00000342175.10:c.52220A>G (TTN)	ENSP00000340554.6:p.Asn17407Ser
ENST00000342992.10:c.71135A>G (TTN)	ENSP00000343764.6:p.Asn23712Ser
ENST00000359218.9:c.52019A>G (TTN)	ENSP00000352154.5:p.Asn17340Ser
ENST00000460472.6:c.51644A>G (TTN)	ENSP00000434586.1:p.Asn17215Ser
ENST00000589042.5:c.78839A>G (TTN) MANE Select	ENSP00000467141.1:p.Asn26280Ser
ENST00000591111.5:c.73916A>G (TTN)	ENSP00000465570.1:p.Asn24639Ser
ENST00000615779.4:c.73916A>G (TTN)	ENSP00000483597.1:p.Asn24639Ser
NM_001256850.1:c.73916A>G (TTN)	NP_001243779.1:p.Asn24639Ser
NM_001267550.2:c.78839A>G (TTN) MANE Select	NP_001254479.2:p.Asn26280Ser
NM_003319.4:c.51644A>G (TTN)	NP_003310.4:p.Asn17215Ser
NM_133378.4:c.71135A>G (TTN)	NP_596869.4:p.Asn23712Ser
NM_133432.3:c.52019A>G (TTN)	NP_597676.3:p.Asn17340Ser
NM_133437.4:c.52220A>G (TTN)	NP_597681.4:p.Asn17407Ser
NR_038271.1:n.447-4007T>C (TTN-AS1)
NR_038272.1:n.2044-15279T>C (TTN-AS1)
XM_011511729.1:c.77936A>G (TTN)	XP_011510031.1:p.Asn25979Ser
XM_011511730.1:c.51830A>G (TTN)	XP_011510032.1:p.Asn17277Ser
XM_011511731.1:c.51689A>G (TTN)	XP_011510033.1:p.Asn17230Ser
XM_017004819.1:c.77732A>G (TTN)	XP_016860308.1:p.Asn25911Ser
XM_017004820.1:c.73130A>G (TTN)	XP_016860309.1:p.Asn24377Ser
XM_017004821.1:c.73127A>G (TTN)	XP_016860310.1:p.Asn24376Ser
XM_017004822.1:c.70169A>G (TTN)	XP_016860311.1:p.Asn23390Ser
XM_017004823.1:c.51785A>G (TTN)	XP_016860312.1:p.Asn17262Ser
XM_024453094.1:c.73280A>G (TTN)	XP_024308862.1:p.Asn24427Ser
XM_024453095.1:c.73277A>G (TTN)	XP_024308863.1:p.Asn24426Ser
XM_024453096.1:c.72710A>G (TTN)	XP_024308864.1:p.Asn24237Ser
XM_024453097.1:c.70052A>G (TTN)	XP_024308865.1:p.Asn23351Ser
XM_024453098.1:c.69971A>G (TTN)	XP_024308866.1:p.Asn23324Ser
XM_024453099.1:c.51734A>G (TTN)	XP_024308867.1:p.Asn17245Ser
XM_024453100.1:c.41588A>G (TTN)	XP_024308868.1:p.Asn13863Ser