Canonical Allele Identifier: CA4783157

Gene: STAU2 STAU2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73421422G>A , CM000670.2:g.73421422G>A	GRCh38
NC_000008.10:g.74333657G>A , CM000670.1:g.74333657G>A	GRCh37
NC_000008.9:g.74496211G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524300.6:c.1663C>T (STAU2) MANE Select	ENSP00000428756.1:p.Pro555Ser
ENST00000521210.5:c.1465C>T (STAU2)	ENSP00000429173.1:p.Pro489Ser
ENST00000522695.5:c.1567C>T (STAU2)	ENSP00000428456.1:p.Pro523Ser
ENST00000522818.1:n.244C>T (STAU2)
ENST00000523558.5:c.1147C>T (STAU2)	ENSP00000428741.1:p.Pro383Ser
ENST00000524300.5:c.1663C>T (STAU2)	ENSP00000428756.1:p.Pro555Ser
NM_001164380.1:c.1663C>T (STAU2)	NP_001157852.1:p.Pro555Ser
NM_001164381.1:c.1567C>T (STAU2)	NP_001157853.1:p.Pro523Ser
NM_001164382.1:c.1465C>T (STAU2)	NP_001157854.1:p.Pro489Ser
NM_001164383.1:c.1147C>T (STAU2)	NP_001157855.1:p.Pro383Ser
NR_038406.1:n.166+1183G>A (STAU2-AS1)
NM_001164380.2:c.1663C>T (STAU2) MANE Select	NP_001157852.1:p.Pro555Ser
NM_001164381.2:c.1567C>T (STAU2)	NP_001157853.1:p.Pro523Ser
NM_001164382.2:c.1465C>T (STAU2)	NP_001157854.1:p.Pro489Ser
NM_001164383.2:c.1147C>T (STAU2)	NP_001157855.1:p.Pro383Ser