Canonical Allele Identifier: CA349411028

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179396601A>G (hg19) ; chr2:g.178531874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178531874A>G , CM000664.2:g.178531874A>G	GRCh38
NC_000002.11:g.179396601A>G , CM000664.1:g.179396601A>G	GRCh37
NC_000002.10:g.179104847A>G	NCBI36
NG_011618.3:g.303929T>C , LRG_391:g.303929T>C
NG_051363.1:g.14048A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.97037T>C (TTN)	ENSP00000343764.6:p.Met32346Thr
ENST00000342175.11:c.78122T>C (TTN)	ENSP00000340554.6:p.Met26041Thr
ENST00000359218.10:c.77921T>C (TTN)	ENSP00000352154.5:p.Met25974Thr
ENST00000342175.10:c.78122T>C (TTN)	ENSP00000340554.6:p.Met26041Thr
ENST00000342992.10:c.97037T>C (TTN)	ENSP00000343764.6:p.Met32346Thr
ENST00000359218.9:c.77921T>C (TTN)	ENSP00000352154.5:p.Met25974Thr
ENST00000460472.6:c.77546T>C (TTN)	ENSP00000434586.1:p.Met25849Thr
ENST00000589042.5:c.104741T>C (TTN) MANE Select	ENSP00000467141.1:p.Met34914Thr
ENST00000591111.5:c.99818T>C (TTN)	ENSP00000465570.1:p.Met33273Thr
ENST00000615779.4:c.99818T>C (TTN)	ENSP00000483597.1:p.Met33273Thr
NM_001256850.1:c.99818T>C (TTN)	NP_001243779.1:p.Met33273Thr
NM_001267550.2:c.104741T>C (TTN) MANE Select	NP_001254479.2:p.Met34914Thr
NM_003319.4:c.77546T>C (TTN)	NP_003310.4:p.Met25849Thr
NM_133378.4:c.97037T>C (TTN)	NP_596869.4:p.Met32346Thr
NM_133432.3:c.77921T>C (TTN)	NP_597676.3:p.Met25974Thr
NM_133437.4:c.78122T>C (TTN)	NP_597681.4:p.Met26041Thr
NR_038271.1:n.446+8238A>G (TTN-AS1)
NR_038272.1:n.220-3858A>G (TTN-AS1)
XM_011511729.1:c.103838T>C (TTN)	XP_011510031.1:p.Met34613Thr
XM_011511730.1:c.77732T>C (TTN)	XP_011510032.1:p.Met25911Thr
XM_011511731.1:c.77591T>C (TTN)	XP_011510033.1:p.Met25864Thr
XM_017004819.1:c.103634T>C (TTN)	XP_016860308.1:p.Met34545Thr
XM_017004820.1:c.99032T>C (TTN)	XP_016860309.1:p.Met33011Thr
XM_017004821.1:c.99029T>C (TTN)	XP_016860310.1:p.Met33010Thr
XM_017004822.1:c.96071T>C (TTN)	XP_016860311.1:p.Met32024Thr
XM_017004823.1:c.77687T>C (TTN)	XP_016860312.1:p.Met25896Thr
XM_024453094.1:c.99182T>C (TTN)	XP_024308862.1:p.Met33061Thr
XM_024453095.1:c.99179T>C (TTN)	XP_024308863.1:p.Met33060Thr
XM_024453096.1:c.98612T>C (TTN)	XP_024308864.1:p.Met32871Thr
XM_024453097.1:c.95954T>C (TTN)	XP_024308865.1:p.Met31985Thr
XM_024453098.1:c.95873T>C (TTN)	XP_024308866.1:p.Met31958Thr
XM_024453099.1:c.77636T>C (TTN)	XP_024308867.1:p.Met25879Thr
XM_024453100.1:c.67490T>C (TTN)	XP_024308868.1:p.Met22497Thr