Canonical Allele Identifier: CA284232

Gene: TTN TTN-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178535209G>C , CM000664.2:g.178535209G>C	GRCh38
NC_000002.11:g.179399936G>C , CM000664.1:g.179399936G>C	GRCh37
NC_000002.10:g.179108182G>C	NCBI36
NG_011618.3:g.300594C>G , LRG_391:g.300594C>G
NG_051363.1:g.17383G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.93702C>G (TTN)	ENSP00000343764.6:p.Val31234=
ENST00000342175.11:c.74787C>G (TTN)	ENSP00000340554.6:p.Val24929=
ENST00000359218.10:c.74586C>G (TTN)	ENSP00000352154.5:p.Val24862=
ENST00000342175.10:c.74787C>G (TTN)	ENSP00000340554.6:p.Val24929=
ENST00000342992.10:c.93702C>G (TTN)	ENSP00000343764.6:p.Val31234=
ENST00000359218.9:c.74586C>G (TTN)	ENSP00000352154.5:p.Val24862=
ENST00000460472.6:c.74211C>G (TTN)	ENSP00000434586.1:p.Val24737=
ENST00000589042.5:c.101406C>G (TTN) MANE Select	ENSP00000467141.1:p.Val33802=
ENST00000591111.5:c.96483C>G (TTN)	ENSP00000465570.1:p.Val32161=
ENST00000615779.4:c.96483C>G (TTN)	ENSP00000483597.1:p.Val32161=
NM_001256850.1:c.96483C>G (TTN)	NP_001243779.1:p.Val32161=
NM_001267550.2:c.101406C>G (TTN) MANE Select	NP_001254479.2:p.Val33802=
NM_003319.4:c.74211C>G (TTN)	NP_003310.4:p.Val24737=
NM_133378.4:c.93702C>G (TTN)	NP_596869.4:p.Val31234=
NM_133432.3:c.74586C>G (TTN)	NP_597676.3:p.Val24862=
NM_133437.4:c.74787C>G (TTN)	NP_597681.4:p.Val24929=
NR_038271.1:n.446+11573G>C (TTN-AS1)
NR_038272.1:n.220-523G>C (TTN-AS1)
XM_011511729.1:c.100503C>G (TTN)	XP_011510031.1:p.Val33501=
XM_011511730.1:c.74397C>G (TTN)	XP_011510032.1:p.Val24799=
XM_011511731.1:c.74256C>G (TTN)	XP_011510033.1:p.Val24752=
XM_017004819.1:c.100299C>G (TTN)	XP_016860308.1:p.Val33433=
XM_017004820.1:c.95697C>G (TTN)	XP_016860309.1:p.Val31899=
XM_017004821.1:c.95694C>G (TTN)	XP_016860310.1:p.Val31898=
XM_017004822.1:c.92736C>G (TTN)	XP_016860311.1:p.Val30912=
XM_017004823.1:c.74352C>G (TTN)	XP_016860312.1:p.Val24784=
XM_024453094.1:c.95847C>G (TTN)	XP_024308862.1:p.Val31949=
XM_024453095.1:c.95844C>G (TTN)	XP_024308863.1:p.Val31948=
XM_024453096.1:c.95277C>G (TTN)	XP_024308864.1:p.Val31759=
XM_024453097.1:c.92619C>G (TTN)	XP_024308865.1:p.Val30873=
XM_024453098.1:c.92538C>G (TTN)	XP_024308866.1:p.Val30846=
XM_024453099.1:c.74301C>G (TTN)	XP_024308867.1:p.Val24767=
XM_024453100.1:c.64155C>G (TTN)	XP_024308868.1:p.Val21385=