Canonical Allele Identifier: CA2667942446
Gene: MRPS22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.139352590T>A , CM000665.2:g.139352590T>A GRCh38
NC_000003.11:g.139071432T>A , CM000665.1:g.139071432T>A GRCh37
NC_000003.10:g.140554122T>A NCBI36
NG_012174.1:g.13572T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000478464.6:c.523-57T>A ENSP00000419303.2:n.523-57T>A
ENST00000480644.2:c.649-57T>A ENSP00000420229.2:n.649-57T>A
ENST00000492644.2:n.2930T>A
ENST00000684961.1:c.352-57T>A ENSP00000508439.1:n.352-57T>A
ENST00000686433.1:c.679-57T>A ENSP00000509173.1:n.679-57T>A
ENST00000687538.1:c.523-57T>A ENSP00000508887.1:n.523-57T>A
ENST00000688697.1:c.733-57T>A ENSP00000510396.1:n.733-57T>A
ENST00000689286.1:c.523-57T>A ENSP00000509897.1:n.523-57T>A
ENST00000689925.1:c.*74-57T>A ENSP00000510082.1:n.*74-57T>A
ENST00000690298.1:c.*374-57T>A ENSP00000509376.1:n.*374-57T>A
ENST00000691070.1:c.649-57T>A ENSP00000509723.1:n.649-57T>A
ENST00000692727.1:n.3255-57T>A
ENST00000693155.1:n.1410-57T>A
ENST00000310776.9:c.730-57T>A ENSP00000310785.5:n.730-57T>A
ENST00000680020.1:c.733-57T>A MANE Select ENSP00000505414.1:n.733-57T>A
ENST00000310776.8:c.733-57T>A ENSP00000310785.4:n.733-57T>A
ENST00000465056.5:c.730-57T>A ENSP00000418233.1:n.730-57T>A
ENST00000478464.5:c.610-57T>A ENSP00000419303.1:n.610-57T>A
ENST00000480644.1:c.218-57T>A
ENST00000480938.5:n.1387-57T>A
ENST00000492644.1:n.1721T>A
ENST00000495075.5:c.733-57T>A ENSP00000418008.1:n.733-57T>A
ENST00000498505.5:c.*330-57T>A ENSP00000420482.1:n.*330-57T>A
NM_020191.2:c.733-57T>A NP_064576.1:n.733-57T>A
XM_005247640.2:c.730-57T>A XP_005247697.1:n.730-57T>A
XM_006713703.2:c.679-57T>A XP_006713766.1:n.679-57T>A
XM_011512995.1:c.610-57T>A XP_011511297.1:n.610-57T>A
XM_011512996.1:c.607-57T>A XP_011511298.1:n.607-57T>A
NM_001363857.1:c.610-57T>A NP_001350786.1:n.610-57T>A
NM_001363893.1:c.730-57T>A NP_001350822.1:n.730-57T>A
NM_020191.3:c.733-57T>A NP_064576.1:n.733-57T>A
XM_006713703.4:c.679-57T>A XP_006713766.1:n.679-57T>A
XM_011512996.2:c.607-57T>A XP_011511298.1:n.607-57T>A
NM_020191.4:c.733-57T>A MANE Select NP_064576.1:n.733-57T>A