Canonical Allele Identifier: CA2595836346

Gene: TSPAN18

Linked Data

• dbSNP Id: rs2135122339
• gnomAD v3: 11-44821624-C-T
• gnomAD v4: 11-44821624-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44821624C>T , CM000673.2:g.44821624C>T	GRCh38
NC_000011.9:g.44843175C>T , CM000673.1:g.44843175C>T	GRCh37
NC_000011.8:g.44799751C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000520358.7:c.-152-38704C>T MANE Select	ENSP00000429993.2:n.-152-38704C>T
ENST00000340160.7:c.-152-38704C>T	ENSP00000339820.3:n.-152-38704C>T
ENST00000520358.6:c.-152-38704C>T	ENSP00000429993.2:n.-152-38704C>T
ENST00000520999.6:c.-199-38704C>T	ENSP00000427942.2:n.-199-38704C>T
ENST00000533080.5:c.-152-38704C>T	ENSP00000433362.1:n.-152-38704C>T
ENST00000533202.5:c.-152-38704C>T	ENSP00000434625.1:n.-152-38704C>T
ENST00000533786.5:c.-152-38704C>T	ENSP00000433592.1:n.-152-38704C>T
NM_130783.4:c.-152-38704C>T	NP_570139.3:n.-152-38704C>T
XM_005253217.2:c.-199-38704C>T	XP_005253274.1:n.-199-38704C>T
XM_006718372.2:c.-199-38704C>T	XP_006718435.1:n.-199-38704C>T
XM_006718373.2:c.-152-38704C>T	XP_006718436.1:n.-152-38704C>T
XM_011520459.1:c.-161-38704C>T	XP_011518761.1:n.-161-38704C>T
XM_005253217.3:c.-199-38704C>T	XP_005253274.1:n.-199-38704C>T
XM_006718372.3:c.-199-38704C>T	XP_006718435.1:n.-199-38704C>T
XM_006718373.4:c.-152-38704C>T	XP_006718436.1:n.-152-38704C>T
XM_011520459.3:c.-161-38704C>T	XP_011518761.1:n.-161-38704C>T
XM_017018530.1:c.-199-38704C>T	XP_016874019.1:n.-199-38704C>T
XM_017018531.1:c.-152-38704C>T	XP_016874020.1:n.-152-38704C>T
NM_130783.5:c.-152-38704C>T MANE Select	NP_570139.3:n.-152-38704C>T