Canonical Allele Identifier: CA179660366

Gene: STAU2 STAU2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73422626C>A , CM000670.2:g.73422626C>A	GRCh38
NC_000008.10:g.74334861C>A , CM000670.1:g.74334861C>A	GRCh37
NC_000008.9:g.74497415C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001164380.2:c.1607G>T (STAU2) MANE Select	NP_001157852.1:p.Gly536Val
ENST00000524300.6:c.1607G>T (STAU2) MANE Select	ENSP00000428756.1:p.Gly536Val
NM_001164380.1:c.1607G>T (STAU2)	NP_001157852.1:p.Gly536Val
NM_001164381.1:c.1511G>T (STAU2)	NP_001157853.1:p.Gly504Val
NM_001164381.2:c.1511G>T (STAU2)	NP_001157853.1:p.Gly504Val
NM_001164382.1:c.1409G>T (STAU2)	NP_001157854.1:p.Gly470Val
NM_001164382.2:c.1409G>T (STAU2)	NP_001157854.1:p.Gly470Val
NM_001164383.1:c.1091G>T (STAU2)	NP_001157855.1:p.Gly364Val
NM_001164383.2:c.1091G>T (STAU2)	NP_001157855.1:p.Gly364Val
NR_038406.1:n.166+2387C>A (STAU2-AS1)
ENST00000521210.5:c.1409G>T (STAU2)	ENSP00000429173.1:p.Gly470Val
ENST00000522695.5:c.1511G>T (STAU2)	ENSP00000428456.1:p.Gly504Val
ENST00000522818.1:n.188G>T (STAU2)
ENST00000523558.5:c.1091G>T (STAU2)	ENSP00000428741.1:p.Gly364Val
ENST00000524300.5:c.1607G>T (STAU2)	ENSP00000428756.1:p.Gly536Val