Canonical Allele Identifier: CA1465349630

Gene: STAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67581435C= , CM000666.2:g.67581435C=	GRCh38
NC_000004.11:g.68447153C= , CM000666.1:g.68447153C=	GRCh37
NC_000004.10:g.68129748C=	NCBI36
NG_047142.1:g.27708C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265404.7:c.494C= MANE Select	ENSP00000265404.2:p.Thr165=
ENST00000265404.6:c.494C=	ENSP00000265404.2:p.Thr165=
ENST00000396225.1:c.494C=	ENSP00000379527.1:p.Thr165=
NM_012108.2:c.494C=	NP_036240.1:p.Thr165=
XM_005265675.3:c.494C=	XP_005265732.1:p.Thr165=
XM_006714175.2:c.494C=	XP_006714238.1:p.Thr165=
XR_427541.2:n.552C=
NM_001317769.1:c.494C=	NP_001304698.1:p.Thr165=
NM_012108.3:c.494C=	NP_036240.1:p.Thr165=
XM_017008018.2:c.494C=	XP_016863507.1:p.Thr165=
NM_012108.4:c.494C= MANE Select	NP_036240.1:p.Thr165=
NM_001317769.2:c.494C=	NP_001304698.1:p.Thr165=