Canonical Allele Identifier: CA349407098

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179395271A>C (hg19) ; chr2:g.178530544A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178530544A>C , CM000664.2:g.178530544A>C	GRCh38
NC_000002.11:g.179395271A>C , CM000664.1:g.179395271A>C	GRCh37
NC_000002.10:g.179103517A>C	NCBI36
NG_011618.3:g.305259T>G , LRG_391:g.305259T>G
NG_051363.1:g.12718A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.98367T>G (TTN)	ENSP00000343764.6:p.Tyr32789Ter
ENST00000342175.11:c.79452T>G (TTN)	ENSP00000340554.6:p.Tyr26484Ter
ENST00000359218.10:c.79251T>G (TTN)	ENSP00000352154.5:p.Tyr26417Ter
ENST00000342175.10:c.79452T>G (TTN)	ENSP00000340554.6:p.Tyr26484Ter
ENST00000342992.10:c.98367T>G (TTN)	ENSP00000343764.6:p.Tyr32789Ter
ENST00000359218.9:c.79251T>G (TTN)	ENSP00000352154.5:p.Tyr26417Ter
ENST00000460472.6:c.78876T>G (TTN)	ENSP00000434586.1:p.Tyr26292Ter
ENST00000589042.5:c.106071T>G (TTN) MANE Select	ENSP00000467141.1:p.Tyr35357Ter
ENST00000591111.5:c.101148T>G (TTN)	ENSP00000465570.1:p.Tyr33716Ter
ENST00000615779.4:c.101148T>G (TTN)	ENSP00000483597.1:p.Tyr33716Ter
NM_001256850.1:c.101148T>G (TTN)	NP_001243779.1:p.Tyr33716Ter
NM_001267550.2:c.106071T>G (TTN) MANE Select	NP_001254479.2:p.Tyr35357Ter
NM_003319.4:c.78876T>G (TTN)	NP_003310.4:p.Tyr26292Ter
NM_133378.4:c.98367T>G (TTN)	NP_596869.4:p.Tyr32789Ter
NM_133432.3:c.79251T>G (TTN)	NP_597676.3:p.Tyr26417Ter
NM_133437.4:c.79452T>G (TTN)	NP_597681.4:p.Tyr26484Ter
NR_038271.1:n.446+6908A>C (TTN-AS1)
NR_038272.1:n.220-5188A>C (TTN-AS1)
XM_011511729.1:c.105168T>G (TTN)	XP_011510031.1:p.Tyr35056Ter
XM_011511730.1:c.79062T>G (TTN)	XP_011510032.1:p.Tyr26354Ter
XM_011511731.1:c.78921T>G (TTN)	XP_011510033.1:p.Tyr26307Ter
XM_017004819.1:c.104964T>G (TTN)	XP_016860308.1:p.Tyr34988Ter
XM_017004820.1:c.100362T>G (TTN)	XP_016860309.1:p.Tyr33454Ter
XM_017004821.1:c.100359T>G (TTN)	XP_016860310.1:p.Tyr33453Ter
XM_017004822.1:c.97401T>G (TTN)	XP_016860311.1:p.Tyr32467Ter
XM_017004823.1:c.79017T>G (TTN)	XP_016860312.1:p.Tyr26339Ter
XM_024453094.1:c.100512T>G (TTN)	XP_024308862.1:p.Tyr33504Ter
XM_024453095.1:c.100509T>G (TTN)	XP_024308863.1:p.Tyr33503Ter
XM_024453096.1:c.99942T>G (TTN)	XP_024308864.1:p.Tyr33314Ter
XM_024453097.1:c.97284T>G (TTN)	XP_024308865.1:p.Tyr32428Ter
XM_024453098.1:c.97203T>G (TTN)	XP_024308866.1:p.Tyr32401Ter
XM_024453099.1:c.78966T>G (TTN)	XP_024308867.1:p.Tyr26322Ter
XM_024453100.1:c.68820T>G (TTN)	XP_024308868.1:p.Tyr22940Ter