Canonical Allele Identifier: CA676801082

Gene: TSPAN18

Linked Data

• dbSNP Id: rs1182779076
• MyVariant Identifiers: chr11:g.44843244_44843255del (hg19) ; chr11:g.44821693_44821704del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44821693_44821704del , CM000673.2:g.44821693_44821704del	GRCh38
NC_000011.9:g.44843244_44843255del , CM000673.1:g.44843244_44843255del	GRCh37
NC_000011.8:g.44799820_44799831del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000520358.7:c.-152-38635_-152-38624del MANE Select	ENSP00000429993.2:n.-152-38635_-152-38624del
ENST00000340160.7:c.-152-38635_-152-38624del	ENSP00000339820.3:n.-152-38635_-152-38624del
ENST00000520358.6:c.-152-38635_-152-38624del	ENSP00000429993.2:n.-152-38635_-152-38624del
ENST00000520999.6:c.-199-38635_-199-38624del	ENSP00000427942.2:n.-199-38635_-199-38624del
ENST00000533080.5:c.-152-38635_-152-38624del	ENSP00000433362.1:n.-152-38635_-152-38624del
ENST00000533202.5:c.-152-38635_-152-38624del	ENSP00000434625.1:n.-152-38635_-152-38624del
ENST00000533786.5:c.-152-38635_-152-38624del	ENSP00000433592.1:n.-152-38635_-152-38624del
NM_130783.4:c.-152-38635_-152-38624del	NP_570139.3:n.-152-38635_-152-38624del
XM_005253217.2:c.-199-38635_-199-38624del	XP_005253274.1:n.-199-38635_-199-38624del
XM_006718372.2:c.-199-38635_-199-38624del	XP_006718435.1:n.-199-38635_-199-38624del
XM_006718373.2:c.-152-38635_-152-38624del	XP_006718436.1:n.-152-38635_-152-38624del
XM_011520459.1:c.-161-38635_-161-38624del	XP_011518761.1:n.-161-38635_-161-38624del
XM_005253217.3:c.-199-38635_-199-38624del	XP_005253274.1:n.-199-38635_-199-38624del
XM_006718372.3:c.-199-38635_-199-38624del	XP_006718435.1:n.-199-38635_-199-38624del
XM_006718373.4:c.-152-38635_-152-38624del	XP_006718436.1:n.-152-38635_-152-38624del
XM_011520459.3:c.-161-38635_-161-38624del	XP_011518761.1:n.-161-38635_-161-38624del
XM_017018530.1:c.-199-38635_-199-38624del	XP_016874019.1:n.-199-38635_-199-38624del
XM_017018531.1:c.-152-38635_-152-38624del	XP_016874020.1:n.-152-38635_-152-38624del
NM_130783.5:c.-152-38635_-152-38624del MANE Select	NP_570139.3:n.-152-38635_-152-38624del