Canonical Allele Identifier: CA357051725
Gene: STAP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67581435C>G , CM000666.2:g.67581435C>G GRCh38
NC_000004.11:g.68447153C>G , CM000666.1:g.68447153C>G GRCh37
NC_000004.10:g.68129748C>G NCBI36
NG_047142.1:g.27708C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000265404.7:c.494C>G MANE Select ENSP00000265404.2:p.Thr165Ser
ENST00000265404.6:c.494C>G ENSP00000265404.2:p.Thr165Ser
ENST00000396225.1:c.494C>G ENSP00000379527.1:p.Thr165Ser
NM_012108.2:c.494C>G NP_036240.1:p.Thr165Ser
XM_005265675.3:c.494C>G XP_005265732.1:p.Thr165Ser
XM_006714175.2:c.494C>G XP_006714238.1:p.Thr165Ser
XR_427541.2:n.552C>G
NM_001317769.1:c.494C>G NP_001304698.1:p.Thr165Ser
NM_012108.3:c.494C>G NP_036240.1:p.Thr165Ser
XM_017008018.2:c.494C>G XP_016863507.1:p.Thr165Ser
NM_012108.4:c.494C>G MANE Select NP_036240.1:p.Thr165Ser
NM_001317769.2:c.494C>G NP_001304698.1:p.Thr165Ser