Canonical Allele Identifier: CA349581330

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179429342G>T (hg19) ; chr2:g.178564615G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178564615G>T , CM000664.2:g.178564615G>T	GRCh38
NC_000002.11:g.179429342G>T , CM000664.1:g.179429342G>T	GRCh37
NC_000002.10:g.179137588G>T	NCBI36
NG_011618.3:g.271188C>A , LRG_391:g.271188C>A
NG_051363.1:g.46789G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.73813C>A (TTN)	ENSP00000343764.6:p.Pro24605Thr
ENST00000342175.11:c.54898C>A (TTN)	ENSP00000340554.6:p.Pro18300Thr
ENST00000359218.10:c.54697C>A (TTN)	ENSP00000352154.5:p.Pro18233Thr
ENST00000342175.10:c.54898C>A (TTN)	ENSP00000340554.6:p.Pro18300Thr
ENST00000342992.10:c.73813C>A (TTN)	ENSP00000343764.6:p.Pro24605Thr
ENST00000359218.9:c.54697C>A (TTN)	ENSP00000352154.5:p.Pro18233Thr
ENST00000460472.6:c.54322C>A (TTN)	ENSP00000434586.1:p.Pro18108Thr
ENST00000589042.5:c.81517C>A (TTN) MANE Select	ENSP00000467141.1:p.Pro27173Thr
ENST00000591111.5:c.76594C>A (TTN)	ENSP00000465570.1:p.Pro25532Thr
ENST00000615779.4:c.76594C>A (TTN)	ENSP00000483597.1:p.Pro25532Thr
NM_001256850.1:c.76594C>A (TTN)	NP_001243779.1:p.Pro25532Thr
NM_001267550.2:c.81517C>A (TTN) MANE Select	NP_001254479.2:p.Pro27173Thr
NM_003319.4:c.54322C>A (TTN)	NP_003310.4:p.Pro18108Thr
NM_133378.4:c.73813C>A (TTN)	NP_596869.4:p.Pro24605Thr
NM_133432.3:c.54697C>A (TTN)	NP_597676.3:p.Pro18233Thr
NM_133437.4:c.54898C>A (TTN)	NP_597681.4:p.Pro18300Thr
NR_038271.1:n.447-6685G>T (TTN-AS1)
NR_038272.1:n.2044-17957G>T (TTN-AS1)
XM_011511729.1:c.80614C>A (TTN)	XP_011510031.1:p.Pro26872Thr
XM_011511730.1:c.54508C>A (TTN)	XP_011510032.1:p.Pro18170Thr
XM_011511731.1:c.54367C>A (TTN)	XP_011510033.1:p.Pro18123Thr
XM_017004819.1:c.80410C>A (TTN)	XP_016860308.1:p.Pro26804Thr
XM_017004820.1:c.75808C>A (TTN)	XP_016860309.1:p.Pro25270Thr
XM_017004821.1:c.75805C>A (TTN)	XP_016860310.1:p.Pro25269Thr
XM_017004822.1:c.72847C>A (TTN)	XP_016860311.1:p.Pro24283Thr
XM_017004823.1:c.54463C>A (TTN)	XP_016860312.1:p.Pro18155Thr
XM_024453094.1:c.75958C>A (TTN)	XP_024308862.1:p.Pro25320Thr
XM_024453095.1:c.75955C>A (TTN)	XP_024308863.1:p.Pro25319Thr
XM_024453096.1:c.75388C>A (TTN)	XP_024308864.1:p.Pro25130Thr
XM_024453097.1:c.72730C>A (TTN)	XP_024308865.1:p.Pro24244Thr
XM_024453098.1:c.72649C>A (TTN)	XP_024308866.1:p.Pro24217Thr
XM_024453099.1:c.54412C>A (TTN)	XP_024308867.1:p.Pro18138Thr
XM_024453100.1:c.44266C>A (TTN)	XP_024308868.1:p.Pro14756Thr