Canonical Allele Identifier: CA1465349635

Gene: STAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67581444A= , CM000666.2:g.67581444A=	GRCh38
NC_000004.11:g.68447162A= , CM000666.1:g.68447162A=	GRCh37
NC_000004.10:g.68129757A=	NCBI36
NG_047142.1:g.27717A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000265404.7:c.503A= MANE Select	ENSP00000265404.2:p.Tyr168=
ENST00000265404.6:c.503A=	ENSP00000265404.2:p.Tyr168=
ENST00000396225.1:c.503A=	ENSP00000379527.1:p.Tyr168=
NM_012108.2:c.503A=	NP_036240.1:p.Tyr168=
XM_005265675.3:c.503A=	XP_005265732.1:p.Tyr168=
XM_006714175.2:c.503A=	XP_006714238.1:p.Tyr168=
XR_427541.2:n.561A=
NM_001317769.1:c.503A=	NP_001304698.1:p.Tyr168=
NM_012108.3:c.503A=	NP_036240.1:p.Tyr168=
XM_017008018.2:c.503A=	XP_016863507.1:p.Tyr168=
NM_012108.4:c.503A= MANE Select	NP_036240.1:p.Tyr168=
NM_001317769.2:c.503A=	NP_001304698.1:p.Tyr168=