Canonical Allele Identifier: CA1738860686

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120810524G= , CM000669.2:g.120810524G=	GRCh38
NC_000007.13:g.120450578G= , CM000669.1:g.120450578G=	GRCh37
NC_000007.12:g.120237814G=	NCBI36
NG_023203.1:g.52600C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.407C= MANE Select	ENSP00000222747.3:p.Thr136=
ENST00000222747.7:c.407C=	ENSP00000222747.3:p.Thr136=
ENST00000415871.5:c.407C=	ENSP00000397699.1:p.Thr136=
ENST00000441017.5:c.407C=	ENSP00000411158.1:p.Thr136=
ENST00000450414.5:c.386C=	ENSP00000397411.1:n.386C=
NM_012338.3:c.407C=	NP_036470.1:p.Thr136=
XM_005250239.1:c.407C=	XP_005250296.1:p.Thr136=
XM_011515993.1:c.407C=	XP_011514295.1:p.Thr136=
XM_011515994.1:c.407C=	XP_011514296.1:p.Thr136=
XM_005250239.3:c.407C=	XP_005250296.1:p.Thr136=
XM_017011913.1:c.332C=	XP_016867402.1:p.Thr111=
NM_012338.4:c.407C= MANE Select	NP_036470.1:p.Thr136=