Canonical Allele Identifier: CA2581422415

Gene: STAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67581531A>T , CM000666.2:g.67581531A>T	GRCh38
NC_000004.11:g.68447249A>T , CM000666.1:g.68447249A>T	GRCh37
NC_000004.10:g.68129844A>T	NCBI36
NG_047142.1:g.27804A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_012108.4:c.530+60A>T MANE Select	NP_036240.1:n.530+60A>T
ENST00000265404.7:c.530+60A>T MANE Select	ENSP00000265404.2:n.530+60A>T
NM_001317769.1:c.530+60A>T	NP_001304698.1:n.530+60A>T
NM_001317769.2:c.530+60A>T	NP_001304698.1:n.530+60A>T
NM_012108.2:c.530+60A>T	NP_036240.1:n.530+60A>T
NM_012108.3:c.530+60A>T	NP_036240.1:n.530+60A>T
ENST00000265404.6:c.530+60A>T	ENSP00000265404.2:n.530+60A>T
ENST00000396225.1:c.530+60A>T	ENSP00000379527.1:n.530+60A>T
XM_005265675.3:c.530+60A>T	XP_005265732.1:n.530+60A>T
XM_006714175.2:c.530+60A>T	XP_006714238.1:n.530+60A>T
XM_017008018.2:c.530+60A>T	XP_016863507.1:n.530+60A>T
XR_427541.2:n.588+60A>T