Canonical Allele Identifier: CA439648632

Gene: STAP1

Linked Data

• MyVariant Identifiers: chr4:g.68447154T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67581436T>A , CM000666.2:g.67581436T>A	GRCh38
NC_000004.11:g.68447154T>A , CM000666.1:g.68447154T>A	GRCh37
NC_000004.10:g.68129749T>A	NCBI36
NG_047142.1:g.27709T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265404.7:c.495T>A MANE Select	ENSP00000265404.2:p.Thr165=
ENST00000265404.6:c.495T>A	ENSP00000265404.2:p.Thr165=
ENST00000396225.1:c.495T>A	ENSP00000379527.1:p.Thr165=
NM_012108.2:c.495T>A	NP_036240.1:p.Thr165=
XM_005265675.3:c.495T>A	XP_005265732.1:p.Thr165=
XM_006714175.2:c.495T>A	XP_006714238.1:p.Thr165=
XR_427541.2:n.553T>A
NM_001317769.1:c.495T>A	NP_001304698.1:p.Thr165=
NM_012108.3:c.495T>A	NP_036240.1:p.Thr165=
XM_017008018.2:c.495T>A	XP_016863507.1:p.Thr165=
NM_012108.4:c.495T>A MANE Select	NP_036240.1:p.Thr165=
NM_001317769.2:c.495T>A	NP_001304698.1:p.Thr165=