Canonical Allele Identifier: CA1738876508
Gene: TSPAN12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120788819C= , CM000669.2:g.120788819C= GRCh38
NC_000007.13:g.120428873C= , CM000669.1:g.120428873C= GRCh37
NC_000007.12:g.120216109C= NCBI36
NG_023203.1:g.74305G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000222747.8:c.691G= MANE Select ENSP00000222747.3:p.Gly231=
ENST00000222747.7:c.691G= ENSP00000222747.3:p.Gly231=
ENST00000415871.5:c.691G= ENSP00000397699.1:p.Gly231=
ENST00000450414.5:c.670G= ENSP00000397411.1:n.670G=
NM_012338.3:c.691G= NP_036470.1:p.Gly231=
XM_005250239.1:c.691G= XP_005250296.1:p.Gly231=
XM_011515993.1:c.691G= XP_011514295.1:p.Gly231=
XM_011515994.1:c.691G= XP_011514296.1:p.Gly231=
XM_005250239.3:c.691G= XP_005250296.1:p.Gly231=
XM_017011913.1:c.616G= XP_016867402.1:p.Gly206=
NM_012338.4:c.691G= MANE Select NP_036470.1:p.Gly231=