Canonical Allele Identifier: CA2045155765

Gene: TSPAN8

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.71151778T= , CM000674.2:g.71151778T=	GRCh38
NC_000012.11:g.71545558T= , CM000674.1:g.71545558T=	GRCh37
NC_000012.10:g.69831825T=	NCBI36
NG_046933.1:g.11222A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004616.3:c.60+5841A= MANE Select	NP_004607.1:n.60+5841A=
ENST00000247829.8:c.60+5841A= MANE Select	ENSP00000247829.3:n.60+5841A=
NM_001369760.1:c.60+5841A=	NP_001356689.1:n.60+5841A=
NM_004616.2:c.60+5841A=	NP_004607.1:n.60+5841A=
ENST00000247829.7:c.60+5841A=	ENSP00000247829.3:n.60+5841A=
ENST00000393330.6:c.60+5841A=	ENSP00000377003.2:n.60+5841A=
ENST00000546561.2:c.60+5841A=	ENSP00000447160.1:n.60+5841A=
ENST00000552786.1:n.319+5122A=
XM_006719583.2:c.60+5841A=	XP_006719646.1:n.60+5841A=
XM_006719583.3:c.60+5841A=	XP_006719646.1:n.60+5841A=
XM_017019913.2:c.60+5841A=	XP_016875402.1:n.60+5841A=