Canonical Allele Identifier: CA349507108

Gene: TTN TTN-AS1

Linked Data

• MyVariant Identifiers: chr2:g.179458752T>G (hg19) ; chr2:g.178594025T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.178594025T>G , CM000664.2:g.178594025T>G	GRCh38
NC_000002.11:g.179458752T>G , CM000664.1:g.179458752T>G	GRCh37
NC_000002.10:g.179166998T>G	NCBI36
NG_011618.3:g.241778A>C , LRG_391:g.241778A>C
NG_051363.1:g.76199T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342992.11:c.50664A>C (TTN)	ENSP00000343764.6:p.Lys16888Asn
ENST00000342175.11:c.31749A>C (TTN)	ENSP00000340554.6:p.Lys10583Asn
ENST00000359218.10:c.31548A>C (TTN)	ENSP00000352154.5:p.Lys10516Asn
ENST00000342175.10:c.31749A>C (TTN)	ENSP00000340554.6:p.Lys10583Asn
ENST00000342992.10:c.50664A>C (TTN)	ENSP00000343764.6:p.Lys16888Asn
ENST00000359218.9:c.31548A>C (TTN)	ENSP00000352154.5:p.Lys10516Asn
ENST00000460472.6:c.31173A>C (TTN)	ENSP00000434586.1:p.Lys10391Asn
ENST00000589042.5:c.58368A>C (TTN) MANE Select	ENSP00000467141.1:p.Lys19456Asn
ENST00000591111.5:c.53445A>C (TTN)	ENSP00000465570.1:p.Lys17815Asn
ENST00000615779.4:c.53445A>C (TTN)	ENSP00000483597.1:p.Lys17815Asn
NM_001256850.1:c.53445A>C (TTN)	NP_001243779.1:p.Lys17815Asn
NM_001267550.2:c.58368A>C (TTN) MANE Select	NP_001254479.2:p.Lys19456Asn
NM_003319.4:c.31173A>C (TTN)	NP_003310.4:p.Lys10391Asn
NM_133378.4:c.50664A>C (TTN)	NP_596869.4:p.Lys16888Asn
NM_133432.3:c.31548A>C (TTN)	NP_597676.3:p.Lys10516Asn
NM_133437.4:c.31749A>C (TTN)	NP_597681.4:p.Lys10583Asn
NR_038271.1:n.597-3571T>G (TTN-AS1)
NR_038272.1:n.3364+2711T>G (TTN-AS1)
XM_011511729.1:c.57465A>C (TTN)	XP_011510031.1:p.Lys19155Asn
XM_011511730.1:c.31359A>C (TTN)	XP_011510032.1:p.Lys10453Asn
XM_011511731.1:c.31218A>C (TTN)	XP_011510033.1:p.Lys10406Asn
XM_017004819.1:c.57261A>C (TTN)	XP_016860308.1:p.Lys19087Asn
XM_017004820.1:c.52659A>C (TTN)	XP_016860309.1:p.Lys17553Asn
XM_017004821.1:c.52656A>C (TTN)	XP_016860310.1:p.Lys17552Asn
XM_017004822.1:c.49698A>C (TTN)	XP_016860311.1:p.Lys16566Asn
XM_017004823.1:c.31314A>C (TTN)	XP_016860312.1:p.Lys10438Asn
XM_024453094.1:c.52809A>C (TTN)	XP_024308862.1:p.Lys17603Asn
XM_024453095.1:c.52806A>C (TTN)	XP_024308863.1:p.Lys17602Asn
XM_024453096.1:c.52239A>C (TTN)	XP_024308864.1:p.Lys17413Asn
XM_024453097.1:c.49581A>C (TTN)	XP_024308865.1:p.Lys16527Asn
XM_024453098.1:c.49500A>C (TTN)	XP_024308866.1:p.Lys16500Asn
XM_024453099.1:c.31263A>C (TTN)	XP_024308867.1:p.Lys10421Asn
XM_024453100.1:c.21117A>C (TTN)	XP_024308868.1:p.Lys7039Asn