Canonical Allele Identifier: CA1968219119

Gene: TSPAN18

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44821612A= , CM000673.2:g.44821612A=	GRCh38
NC_000011.9:g.44843163A= , CM000673.1:g.44843163A=	GRCh37
NC_000011.8:g.44799739A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000520358.7:c.-152-38716A= MANE Select	ENSP00000429993.2:n.-152-38716A=
ENST00000340160.7:c.-152-38716A=	ENSP00000339820.3:n.-152-38716A=
ENST00000520358.6:c.-152-38716A=	ENSP00000429993.2:n.-152-38716A=
ENST00000520999.6:c.-199-38716A=	ENSP00000427942.2:n.-199-38716A=
ENST00000533080.5:c.-152-38716A=	ENSP00000433362.1:n.-152-38716A=
ENST00000533202.5:c.-152-38716A=	ENSP00000434625.1:n.-152-38716A=
ENST00000533786.5:c.-152-38716A=	ENSP00000433592.1:n.-152-38716A=
NM_130783.4:c.-152-38716A=	NP_570139.3:n.-152-38716A=
XM_005253217.2:c.-199-38716A=	XP_005253274.1:n.-199-38716A=
XM_006718372.2:c.-199-38716A=	XP_006718435.1:n.-199-38716A=
XM_006718373.2:c.-152-38716A=	XP_006718436.1:n.-152-38716A=
XM_011520459.1:c.-161-38716A=	XP_011518761.1:n.-161-38716A=
XM_005253217.3:c.-199-38716A=	XP_005253274.1:n.-199-38716A=
XM_006718372.3:c.-199-38716A=	XP_006718435.1:n.-199-38716A=
XM_006718373.4:c.-152-38716A=	XP_006718436.1:n.-152-38716A=
XM_011520459.3:c.-161-38716A=	XP_011518761.1:n.-161-38716A=
XM_017018530.1:c.-199-38716A=	XP_016874019.1:n.-199-38716A=
XM_017018531.1:c.-152-38716A=	XP_016874020.1:n.-152-38716A=
NM_130783.5:c.-152-38716A= MANE Select	NP_570139.3:n.-152-38716A=