Canonical Allele Identifier: CA2663063185

Gene: TNS1

Linked Data - Sequence & Population

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.217835886del , CM000664.2:g.217835886del	GRCh38
NC_000002.11:g.218700609del , CM000664.1:g.218700609del	GRCh37
NC_000002.10:g.218408854del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000419504.6:c.2829+131del	ENSP00000408724.1:n.2829+131del
ENST00000615025.6:c.2829+131del	ENSP00000480559.2:n.2829+131del
ENST00000705226.1:c.2916+131del	ENSP00000516092.1:n.2916+131del
ENST00000615025.5:c.2829+131del	ENSP00000480559.2:n.2829+131del
ENST00000682258.1:c.3204+131del MANE Select	ENSP00000506917.1:n.3204+131del
ENST00000646520.1:c.3267+131del	ENSP00000493967.1:n.3267+131del
ENST00000651849.1:c.3129+131del	ENSP00000498399.1:n.3129+131del
ENST00000171887.8:c.2829+131del	ENSP00000171887.4:n.2829+131del
ENST00000419504.5:c.2829+131del	ENSP00000408724.1:n.2829+131del
ENST00000430930.5:c.2829+131del	ENSP00000406016.1:n.2829+131del
ENST00000446688.5:c.225+131del	ENSP00000394171.2:n.225+131del
ENST00000611415.4:c.2829+131del	ENSP00000484271.1:n.2829+131del
ENST00000615025.4:c.1782+131del	ENSP00000480559.1:n.1782+131del
NM_001308022.1:c.2829+131del	NP_001294951.1:n.2829+131del
NM_001308023.1:c.2829+131del	NP_001294952.1:n.2829+131del
NM_022648.4:c.2829+131del	NP_072174.3:n.2829+131del
NM_022648.5:c.2829+131del	NP_072174.3:n.2829+131del
XM_011511711.1:c.3180+131del	XP_011510013.1:n.3180+131del
XM_011511712.1:c.3180+131del	XP_011510014.1:n.3180+131del
XM_011511713.1:c.3180+131del	XP_011510015.1:n.3180+131del
XM_011511714.1:c.3132+131del	XP_011510016.1:n.3132+131del
XM_011511715.1:c.3180+131del	XP_011510017.1:n.3180+131del
XM_011511716.1:c.3093+131del	XP_011510018.1:n.3093+131del
XM_011511717.1:c.2964+131del	XP_011510019.1:n.2964+131del
XM_011511718.1:c.2916+131del	XP_011510020.1:n.2916+131del
XM_011511721.1:c.3180+131del	XP_011510023.1:n.3180+131del
XM_011511722.1:c.3180+131del	XP_011510024.1:n.3180+131del
XM_011511723.1:c.2829+131del	XP_011510025.1:n.2829+131del
XM_011511724.1:c.2046+131del	XP_011510026.1:n.2046+131del
XM_011511725.1:c.2001+131del	XP_011510027.1:n.2001+131del
XM_011511726.1:c.1548+131del	XP_011510028.1:n.1548+131del
XM_011511727.1:c.225+131del	XP_011510029.1:n.225+131del
XM_011511728.1:c.225+131del	XP_011510030.1:n.225+131del
XR_923002.1:n.3234+131del
XM_011511723.2:c.2829+131del	XP_011510025.1:n.2829+131del
XM_017004811.1:c.2916+131del	XP_016860300.1:n.2916+131del
XM_017004812.1:c.2916+131del	XP_016860301.1:n.2916+131del
XM_017004813.2:c.2046+131del	XP_016860302.1:n.2046+131del
XM_017004814.1:c.1548+131del	XP_016860303.1:n.1548+131del
XM_017004815.1:c.1548+131del	XP_016860304.1:n.1548+131del
XM_024453068.1:c.3132+131del	XP_024308836.1:n.3132+131del
XM_024453069.1:c.3045+131del	XP_024308837.1:n.3045+131del
XM_024453070.1:c.3132+131del	XP_024308838.1:n.3132+131del
XM_024453071.1:c.3132+131del	XP_024308839.1:n.3132+131del
XM_024453072.1:c.2964+131del	XP_024308840.1:n.2964+131del
XM_024453073.1:c.3132+131del	XP_024308841.1:n.3132+131del
XM_024453074.1:c.3132+131del	XP_024308842.1:n.3132+131del
XM_024453075.1:c.3045+131del	XP_024308843.1:n.3045+131del
XM_024453076.1:c.3045+131del	XP_024308844.1:n.3045+131del
XM_024453077.1:c.2829+131del	XP_024308845.1:n.2829+131del
XM_024453078.1:c.2916+131del	XP_024308846.1:n.2916+131del
XM_024453079.1:c.3507+131del	XP_024308847.1:n.3507+131del
XM_024453080.1:c.3327+131del	XP_024308848.1:n.3327+131del
XM_024453081.1:c.3132+131del	XP_024308849.1:n.3132+131del
XM_024453082.1:c.3132+131del	XP_024308850.1:n.3132+131del
XM_024453083.1:c.3204+131del	XP_024308851.1:n.3204+131del
XM_024453084.1:c.2829+131del	XP_024308852.1:n.2829+131del
NM_001308023.2:c.2829+131del	NP_001294952.1:n.2829+131del
NM_022648.6:c.2829+131del	NP_072174.3:n.2829+131del
NM_001308022.2:c.2829+131del	NP_001294951.1:n.2829+131del
NM_001387777.1:c.3204+131del MANE Select	NP_001374706.1:n.3204+131del
NM_022648.7:c.2829+131del	NP_072174.3:n.2829+131del