Canonical Allele Identifier: CA239490105
Gene: TSPAN8 HGNC NCBI

Linked Data

dbSNP Id: rs1705236

Genomic Alleles

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

Transcript Alleles

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