Canonical Allele Identifier: CA1405583062
Gene: MRPS22 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.139346956G= , CM000665.2:g.139346956G= GRCh38
NC_000003.11:g.139065798G= , CM000665.1:g.139065798G= GRCh37
NC_000003.10:g.140548488G= NCBI36
NG_012174.1:g.7938G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478464.6:c.41G= ENSP00000419303.2:p.Gly14=
ENST00000480644.2:c.251G= ENSP00000420229.2:p.Gly84=
ENST00000492644.2:n.265G=
ENST00000684961.1:c.-42-1204G= ENSP00000508439.1:n.-42-1204G=
ENST00000686433.1:c.251G= ENSP00000509173.1:p.Gly84=
ENST00000687538.1:c.41G= ENSP00000508887.1:p.Gly14=
ENST00000688697.1:c.251G= ENSP00000510396.1:p.Gly84=
ENST00000689286.1:c.41G= ENSP00000509897.1:p.Gly14=
ENST00000689925.1:c.41G= ENSP00000510082.1:p.Gly14=
ENST00000690298.1:c.173-1204G= ENSP00000509376.1:n.173-1204G=
ENST00000691070.1:c.251G= ENSP00000509723.1:p.Gly84=
ENST00000692727.1:n.265G=
ENST00000693155.1:n.274G=
ENST00000310776.9:c.248G= ENSP00000310785.5:p.Gly83=
ENST00000680020.1:c.251G= MANE Select ENSP00000505414.1:p.Gly84=
ENST00000310776.8:c.251G= ENSP00000310785.4:p.Gly84=
ENST00000465056.5:c.248G= ENSP00000418233.1:p.Gly83=
ENST00000465373.5:c.266G= ENSP00000419920.1:p.Gly89=
ENST00000466690.5:c.237G=
ENST00000478464.5:c.128G= ENSP00000419303.1:p.Gly43=
ENST00000480938.5:n.251G=
ENST00000486705.1:n.162G=
ENST00000495075.5:c.251G= ENSP00000418008.1:p.Gly84=
ENST00000498505.5:c.248G= ENSP00000420482.1:p.Gly83=
NM_020191.2:c.251G= NP_064576.1:p.Gly84=
XM_005247640.2:c.248G= XP_005247697.1:p.Gly83=
XM_006713703.2:c.251G= XP_006713766.1:p.Gly84=
XM_011512995.1:c.128G= XP_011511297.1:p.Gly43=
XM_011512996.1:c.125G= XP_011511298.1:p.Gly42=
NM_001363857.1:c.128G= NP_001350786.1:p.Gly43=
NM_001363893.1:c.248G= NP_001350822.1:p.Gly83=
NM_020191.3:c.251G= NP_064576.1:p.Gly84=
XM_006713703.4:c.251G= XP_006713766.1:p.Gly84=
XM_011512996.2:c.125G= XP_011511298.1:p.Gly42=
NM_020191.4:c.251G= MANE Select NP_064576.1:p.Gly84=