Canonical Allele Identifier: CA309235

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178612567G>C , CM000664.2:g.178612567G>C	GRCh38
NC_000002.11:g.179477294G>C , CM000664.1:g.179477294G>C	GRCh37
NC_000002.10:g.179185539G>C	NCBI36
NG_011618.3:g.223236C>G , LRG_391:g.223236C>G
NG_051363.1:g.94741G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001267550.2:c.49958C>G (TTN) MANE Select	NP_001254479.2:p.Ser16653Ter
ENST00000589042.5:c.49958C>G (TTN) MANE Select	ENSP00000467141.1:p.Ser16653Ter
NM_001256850.1:c.45035C>G (TTN)	NP_001243779.1:p.Ser15012Ter
NM_003319.4:c.22763C>G (TTN)	NP_003310.4:p.Ser7588Ter
NM_133378.4:c.42254C>G (TTN)	NP_596869.4:p.Ser14085Ter
NM_133432.3:c.23138C>G (TTN)	NP_597676.3:p.Ser7713Ter
NM_133437.4:c.23339C>G (TTN)	NP_597681.4:p.Ser7780Ter
NR_038271.1:n.783-1468G>C (TTN-AS1)
ENST00000342175.10:c.23339C>G (TTN)	ENSP00000340554.6:p.Ser7780Ter
ENST00000342175.11:c.23339C>G (TTN)	ENSP00000340554.6:p.Ser7780Ter
ENST00000342992.10:c.42254C>G (TTN)	ENSP00000343764.6:p.Ser14085Ter
ENST00000342992.11:c.42254C>G (TTN)	ENSP00000343764.6:p.Ser14085Ter
ENST00000359218.10:c.23138C>G (TTN)	ENSP00000352154.5:p.Ser7713Ter
ENST00000359218.9:c.23138C>G (TTN)	ENSP00000352154.5:p.Ser7713Ter
ENST00000460472.6:c.22763C>G (TTN)	ENSP00000434586.1:p.Ser7588Ter
ENST00000591111.5:c.45035C>G (TTN)	ENSP00000465570.1:p.Ser15012Ter
ENST00000615779.4:c.45035C>G (TTN)	ENSP00000483597.1:p.Ser15012Ter
XM_011511729.1:c.49055C>G (TTN)	XP_011510031.1:p.Ser16352Ter
XM_011511730.1:c.22949C>G (TTN)	XP_011510032.1:p.Ser7650Ter
XM_011511731.1:c.22808C>G (TTN)	XP_011510033.1:p.Ser7603Ter
XM_017004819.1:c.48851C>G (TTN)	XP_016860308.1:p.Ser16284Ter
XM_017004820.1:c.44249C>G (TTN)	XP_016860309.1:p.Ser14750Ter
XM_017004821.1:c.44246C>G (TTN)	XP_016860310.1:p.Ser14749Ter
XM_017004822.1:c.41288C>G (TTN)	XP_016860311.1:p.Ser13763Ter
XM_017004823.1:c.22904C>G (TTN)	XP_016860312.1:p.Ser7635Ter
XM_024453094.1:c.44399C>G (TTN)	XP_024308862.1:p.Ser14800Ter
XM_024453095.1:c.44396C>G (TTN)	XP_024308863.1:p.Ser14799Ter
XM_024453096.1:c.43829C>G (TTN)	XP_024308864.1:p.Ser14610Ter
XM_024453097.1:c.41171C>G (TTN)	XP_024308865.1:p.Ser13724Ter
XM_024453098.1:c.41090C>G (TTN)	XP_024308866.1:p.Ser13697Ter
XM_024453099.1:c.22853C>G (TTN)	XP_024308867.1:p.Ser7618Ter
XM_024453100.1:c.12707C>G (TTN)	XP_024308868.1:p.Ser4236Ter