Canonical Allele Identifier: CA4783221

Gene: STAU2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73552118G>T , CM000670.2:g.73552118G>T	GRCh38
NC_000008.10:g.74464353G>T , CM000670.1:g.74464353G>T	GRCh37
NC_000008.9:g.74626907G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000524300.6:c.1424C>A MANE Select	ENSP00000428756.1:p.Ser475Tyr
ENST00000355780.9:c.1328C>A	ENSP00000348026.5:p.Ser443Tyr
ENST00000517542.5:c.1310C>A	ENSP00000431111.1:p.Ser437Tyr
ENST00000518767.5:c.908C>A	ENSP00000429005.1:p.Ser303Tyr
ENST00000518981.5:c.*320C>A	ENSP00000428664.1:n.*320C>A
ENST00000519961.5:c.1424C>A	ENSP00000430907.1:p.Ser475Tyr
ENST00000521210.5:c.1112C>A	ENSP00000429173.1:p.Ser371Tyr
ENST00000521451.5:c.764C>A	ENSP00000428476.1:p.Ser255Tyr
ENST00000521727.5:c.1364C>A	ENSP00000429973.1:p.Ser455Tyr
ENST00000522509.5:c.1328C>A	ENSP00000427977.1:p.Ser443Tyr
ENST00000522695.5:c.1328C>A	ENSP00000428456.1:p.Ser443Tyr
ENST00000523533.5:c.263C>A	ENSP00000430511.1:p.Ser88Tyr
ENST00000523558.5:c.908C>A	ENSP00000428741.1:p.Ser303Tyr
ENST00000524300.5:c.1424C>A	ENSP00000428756.1:p.Ser475Tyr
NM_001164380.1:c.1424C>A	NP_001157852.1:p.Ser475Tyr
NM_001164381.1:c.1328C>A	NP_001157853.1:p.Ser443Tyr
NM_001164382.1:c.1112C>A	NP_001157854.1:p.Ser371Tyr
NM_001164383.1:c.908C>A	NP_001157855.1:p.Ser303Tyr
NM_001164384.1:c.1328C>A	NP_001157856.1:p.Ser443Tyr
NM_001164385.1:c.1310C>A	NP_001157857.1:p.Ser437Tyr
NM_014393.2:c.1328C>A	NP_055208.2:p.Ser443Tyr
NM_001164380.2:c.1424C>A MANE Select	NP_001157852.1:p.Ser475Tyr
NM_001164381.2:c.1328C>A	NP_001157853.1:p.Ser443Tyr
NM_001164382.2:c.1112C>A	NP_001157854.1:p.Ser371Tyr
NM_001164383.2:c.908C>A	NP_001157855.1:p.Ser303Tyr
NM_001164384.2:c.1328C>A	NP_001157856.1:p.Ser443Tyr
NM_001164385.2:c.1310C>A	NP_001157857.1:p.Ser437Tyr
NM_014393.3:c.1328C>A	NP_055208.2:p.Ser443Tyr