Canonical Allele Identifier: CA1465349681

Gene: STAP1

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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