Canonical Allele Identifier: CA357051838

Gene: STAP1

Linked Data

• gnomAD v4: 4-67581444-A-T
• MyVariant Identifiers: chr4:g.68447162A>T (hg19) ; chr4:g.67581444A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265404.7:c.503A>T MANE Select	ENSP00000265404.2:p.Tyr168Phe
ENST00000265404.6:c.503A>T	ENSP00000265404.2:p.Tyr168Phe
ENST00000396225.1:c.503A>T	ENSP00000379527.1:p.Tyr168Phe
NM_012108.2:c.503A>T	NP_036240.1:p.Tyr168Phe
XM_005265675.3:c.503A>T	XP_005265732.1:p.Tyr168Phe
XM_006714175.2:c.503A>T	XP_006714238.1:p.Tyr168Phe
XR_427541.2:n.561A>T
NM_001317769.1:c.503A>T	NP_001304698.1:p.Tyr168Phe
NM_012108.3:c.503A>T	NP_036240.1:p.Tyr168Phe
XM_017008018.2:c.503A>T	XP_016863507.1:p.Tyr168Phe
NM_012108.4:c.503A>T MANE Select	NP_036240.1:p.Tyr168Phe
NM_001317769.2:c.503A>T	NP_001304698.1:p.Tyr168Phe