Canonical Allele Identifier: CA349427109

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179401895G>C (hg19) ; chr2:g.178537168G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178537168G>C , CM000664.2:g.178537168G>C	GRCh38
NC_000002.11:g.179401895G>C , CM000664.1:g.179401895G>C	GRCh37
NC_000002.10:g.179110141G>C	NCBI36
NG_011618.3:g.298635C>G , LRG_391:g.298635C>G
NG_051363.1:g.19342G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000342992.11:c.92237C>G (TTN)	ENSP00000343764.6:p.Pro30746Arg
ENST00000342175.11:c.73322C>G (TTN)	ENSP00000340554.6:p.Pro24441Arg
ENST00000359218.10:c.73121C>G (TTN)	ENSP00000352154.5:p.Pro24374Arg
ENST00000342175.10:c.73322C>G (TTN)	ENSP00000340554.6:p.Pro24441Arg
ENST00000342992.10:c.92237C>G (TTN)	ENSP00000343764.6:p.Pro30746Arg
ENST00000359218.9:c.73121C>G (TTN)	ENSP00000352154.5:p.Pro24374Arg
ENST00000460472.6:c.72746C>G (TTN)	ENSP00000434586.1:p.Pro24249Arg
ENST00000589042.5:c.99941C>G (TTN) MANE Select	ENSP00000467141.1:p.Pro33314Arg
ENST00000591111.5:c.95018C>G (TTN)	ENSP00000465570.1:p.Pro31673Arg
ENST00000615779.4:c.95018C>G (TTN)	ENSP00000483597.1:p.Pro31673Arg
NM_001256850.1:c.95018C>G (TTN)	NP_001243779.1:p.Pro31673Arg
NM_001267550.2:c.99941C>G (TTN) MANE Select	NP_001254479.2:p.Pro33314Arg
NM_003319.4:c.72746C>G (TTN)	NP_003310.4:p.Pro24249Arg
NM_133378.4:c.92237C>G (TTN)	NP_596869.4:p.Pro30746Arg
NM_133432.3:c.73121C>G (TTN)	NP_597676.3:p.Pro24374Arg
NM_133437.4:c.73322C>G (TTN)	NP_597681.4:p.Pro24441Arg
NR_038271.1:n.446+13532G>C (TTN-AS1)
NR_038272.1:n.317-193G>C (TTN-AS1)
XM_011511729.1:c.99038C>G (TTN)	XP_011510031.1:p.Pro33013Arg
XM_011511730.1:c.72932C>G (TTN)	XP_011510032.1:p.Pro24311Arg
XM_011511731.1:c.72791C>G (TTN)	XP_011510033.1:p.Pro24264Arg
XM_017004819.1:c.98834C>G (TTN)	XP_016860308.1:p.Pro32945Arg
XM_017004820.1:c.94232C>G (TTN)	XP_016860309.1:p.Pro31411Arg
XM_017004821.1:c.94229C>G (TTN)	XP_016860310.1:p.Pro31410Arg
XM_017004822.1:c.91271C>G (TTN)	XP_016860311.1:p.Pro30424Arg
XM_017004823.1:c.72887C>G (TTN)	XP_016860312.1:p.Pro24296Arg
XM_024453094.1:c.94382C>G (TTN)	XP_024308862.1:p.Pro31461Arg
XM_024453095.1:c.94379C>G (TTN)	XP_024308863.1:p.Pro31460Arg
XM_024453096.1:c.93812C>G (TTN)	XP_024308864.1:p.Pro31271Arg
XM_024453097.1:c.91154C>G (TTN)	XP_024308865.1:p.Pro30385Arg
XM_024453098.1:c.91073C>G (TTN)	XP_024308866.1:p.Pro30358Arg
XM_024453099.1:c.72836C>G (TTN)	XP_024308867.1:p.Pro24279Arg
XM_024453100.1:c.62690C>G (TTN)	XP_024308868.1:p.Pro20897Arg