Canonical Allele Identifier: CA349581322

Gene: TTN TTN-AS1

Linked Data

• gnomAD v4: 2-178564611-G-C
• MyVariant Identifiers: chr2:g.179429338G>C (hg19) ; chr2:g.178564611G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178564611G>C , CM000664.2:g.178564611G>C	GRCh38
NC_000002.11:g.179429338G>C , CM000664.1:g.179429338G>C	GRCh37
NC_000002.10:g.179137584G>C	NCBI36
NG_011618.3:g.271192C>G , LRG_391:g.271192C>G
NG_051363.1:g.46785G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.73817C>G (TTN)	ENSP00000343764.6:p.Pro24606Arg
ENST00000342175.11:c.54902C>G (TTN)	ENSP00000340554.6:p.Pro18301Arg
ENST00000359218.10:c.54701C>G (TTN)	ENSP00000352154.5:p.Pro18234Arg
ENST00000342175.10:c.54902C>G (TTN)	ENSP00000340554.6:p.Pro18301Arg
ENST00000342992.10:c.73817C>G (TTN)	ENSP00000343764.6:p.Pro24606Arg
ENST00000359218.9:c.54701C>G (TTN)	ENSP00000352154.5:p.Pro18234Arg
ENST00000460472.6:c.54326C>G (TTN)	ENSP00000434586.1:p.Pro18109Arg
ENST00000589042.5:c.81521C>G (TTN) MANE Select	ENSP00000467141.1:p.Pro27174Arg
ENST00000591111.5:c.76598C>G (TTN)	ENSP00000465570.1:p.Pro25533Arg
ENST00000615779.4:c.76598C>G (TTN)	ENSP00000483597.1:p.Pro25533Arg
NM_001256850.1:c.76598C>G (TTN)	NP_001243779.1:p.Pro25533Arg
NM_001267550.2:c.81521C>G (TTN) MANE Select	NP_001254479.2:p.Pro27174Arg
NM_003319.4:c.54326C>G (TTN)	NP_003310.4:p.Pro18109Arg
NM_133378.4:c.73817C>G (TTN)	NP_596869.4:p.Pro24606Arg
NM_133432.3:c.54701C>G (TTN)	NP_597676.3:p.Pro18234Arg
NM_133437.4:c.54902C>G (TTN)	NP_597681.4:p.Pro18301Arg
NR_038271.1:n.447-6689G>C (TTN-AS1)
NR_038272.1:n.2044-17961G>C (TTN-AS1)
XM_011511729.1:c.80618C>G (TTN)	XP_011510031.1:p.Pro26873Arg
XM_011511730.1:c.54512C>G (TTN)	XP_011510032.1:p.Pro18171Arg
XM_011511731.1:c.54371C>G (TTN)	XP_011510033.1:p.Pro18124Arg
XM_017004819.1:c.80414C>G (TTN)	XP_016860308.1:p.Pro26805Arg
XM_017004820.1:c.75812C>G (TTN)	XP_016860309.1:p.Pro25271Arg
XM_017004821.1:c.75809C>G (TTN)	XP_016860310.1:p.Pro25270Arg
XM_017004822.1:c.72851C>G (TTN)	XP_016860311.1:p.Pro24284Arg
XM_017004823.1:c.54467C>G (TTN)	XP_016860312.1:p.Pro18156Arg
XM_024453094.1:c.75962C>G (TTN)	XP_024308862.1:p.Pro25321Arg
XM_024453095.1:c.75959C>G (TTN)	XP_024308863.1:p.Pro25320Arg
XM_024453096.1:c.75392C>G (TTN)	XP_024308864.1:p.Pro25131Arg
XM_024453097.1:c.72734C>G (TTN)	XP_024308865.1:p.Pro24245Arg
XM_024453098.1:c.72653C>G (TTN)	XP_024308866.1:p.Pro24218Arg
XM_024453099.1:c.54416C>G (TTN)	XP_024308867.1:p.Pro18139Arg
XM_024453100.1:c.44270C>G (TTN)	XP_024308868.1:p.Pro14757Arg