Canonical Allele Identifier: CA2577918613
Gene: MRPS22 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.139344288C>A , CM000665.2:g.139344288C>A GRCh38
NC_000003.11:g.139063130C>A , CM000665.1:g.139063130C>A GRCh37
NC_000003.10:g.140545820C>A NCBI36
NG_012174.1:g.5270C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000480644.2:c.172+90C>A ENSP00000420229.2:n.172+90C>A
ENST00000492644.2:n.186+90C>A
ENST00000684961.1:c.-42-3872C>A ENSP00000508439.1:n.-42-3872C>A
ENST00000686433.1:c.172+90C>A ENSP00000509173.1:n.172+90C>A
ENST00000687538.1:c.-38-2590C>A ENSP00000508887.1:n.-38-2590C>A
ENST00000688697.1:c.172+90C>A ENSP00000510396.1:n.172+90C>A
ENST00000690298.1:c.172+90C>A ENSP00000509376.1:n.172+90C>A
ENST00000691070.1:c.172+90C>A ENSP00000509723.1:n.172+90C>A
ENST00000692727.1:n.186+90C>A
ENST00000693155.1:n.195+90C>A
ENST00000310776.9:c.172+90C>A ENSP00000310785.5:n.172+90C>A
ENST00000680020.1:c.172+90C>A MANE Select ENSP00000505414.1:n.172+90C>A
ENST00000310776.8:c.172+90C>A ENSP00000310785.4:n.172+90C>A
ENST00000465056.5:c.172+90C>A ENSP00000418233.1:n.172+90C>A
ENST00000465373.5:c.160+90C>A ENSP00000419920.1:n.160+90C>A
ENST00000466690.5:c.158+90C>A
ENST00000480938.5:n.172+90C>A
ENST00000486705.1:n.83+90C>A
ENST00000495075.5:c.172+90C>A ENSP00000418008.1:n.172+90C>A
ENST00000495225.1:c.83-2590C>A ENSP00000417104.1:n.83-2590C>A
ENST00000498505.5:c.172+90C>A ENSP00000420482.1:n.172+90C>A
NM_020191.2:c.172+90C>A NP_064576.1:n.172+90C>A
XM_005247640.2:c.172+90C>A XP_005247697.1:n.172+90C>A
XM_006713703.2:c.172+90C>A XP_006713766.1:n.172+90C>A
NM_001363893.1:c.172+90C>A NP_001350822.1:n.172+90C>A
NM_020191.3:c.172+90C>A NP_064576.1:n.172+90C>A
XM_006713703.4:c.172+90C>A XP_006713766.1:n.172+90C>A
NM_020191.4:c.172+90C>A MANE Select NP_064576.1:n.172+90C>A