Canonical Allele Identifier: CA349581325

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179429339G>T (hg19) ; chr2:g.178564612G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178564612G>T , CM000664.2:g.178564612G>T	GRCh38
NC_000002.11:g.179429339G>T , CM000664.1:g.179429339G>T	GRCh37
NC_000002.10:g.179137585G>T	NCBI36
NG_011618.3:g.271191C>A , LRG_391:g.271191C>A
NG_051363.1:g.46786G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.73816C>A (TTN)	ENSP00000343764.6:p.Pro24606Thr
ENST00000342175.11:c.54901C>A (TTN)	ENSP00000340554.6:p.Pro18301Thr
ENST00000359218.10:c.54700C>A (TTN)	ENSP00000352154.5:p.Pro18234Thr
ENST00000342175.10:c.54901C>A (TTN)	ENSP00000340554.6:p.Pro18301Thr
ENST00000342992.10:c.73816C>A (TTN)	ENSP00000343764.6:p.Pro24606Thr
ENST00000359218.9:c.54700C>A (TTN)	ENSP00000352154.5:p.Pro18234Thr
ENST00000460472.6:c.54325C>A (TTN)	ENSP00000434586.1:p.Pro18109Thr
ENST00000589042.5:c.81520C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro27174Thr
ENST00000591111.5:c.76597C>A (TTN)	ENSP00000465570.1:p.Pro25533Thr
ENST00000615779.4:c.76597C>A (TTN)	ENSP00000483597.1:p.Pro25533Thr
NM_001256850.1:c.76597C>A (TTN)	NP_001243779.1:p.Pro25533Thr
NM_001267550.2:c.81520C>A (TTN) MANE Select	NP_001254479.2:p.Pro27174Thr
NM_003319.4:c.54325C>A (TTN)	NP_003310.4:p.Pro18109Thr
NM_133378.4:c.73816C>A (TTN)	NP_596869.4:p.Pro24606Thr
NM_133432.3:c.54700C>A (TTN)	NP_597676.3:p.Pro18234Thr
NM_133437.4:c.54901C>A (TTN)	NP_597681.4:p.Pro18301Thr
NR_038271.1:n.447-6688G>T (TTN-AS1)
NR_038272.1:n.2044-17960G>T (TTN-AS1)
XM_011511729.1:c.80617C>A (TTN)	XP_011510031.1:p.Pro26873Thr
XM_011511730.1:c.54511C>A (TTN)	XP_011510032.1:p.Pro18171Thr
XM_011511731.1:c.54370C>A (TTN)	XP_011510033.1:p.Pro18124Thr
XM_017004819.1:c.80413C>A (TTN)	XP_016860308.1:p.Pro26805Thr
XM_017004820.1:c.75811C>A (TTN)	XP_016860309.1:p.Pro25271Thr
XM_017004821.1:c.75808C>A (TTN)	XP_016860310.1:p.Pro25270Thr
XM_017004822.1:c.72850C>A (TTN)	XP_016860311.1:p.Pro24284Thr
XM_017004823.1:c.54466C>A (TTN)	XP_016860312.1:p.Pro18156Thr
XM_024453094.1:c.75961C>A (TTN)	XP_024308862.1:p.Pro25321Thr
XM_024453095.1:c.75958C>A (TTN)	XP_024308863.1:p.Pro25320Thr
XM_024453096.1:c.75391C>A (TTN)	XP_024308864.1:p.Pro25131Thr
XM_024453097.1:c.72733C>A (TTN)	XP_024308865.1:p.Pro24245Thr
XM_024453098.1:c.72652C>A (TTN)	XP_024308866.1:p.Pro24218Thr
XM_024453099.1:c.54415C>A (TTN)	XP_024308867.1:p.Pro18139Thr
XM_024453100.1:c.44269C>A (TTN)	XP_024308868.1:p.Pro14757Thr