Canonical Allele Identifier: CA435876056

Gene: MRPS22

Linked Data

• MyVariant Identifiers: chr3:g.139065820T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.139346978T>C , CM000665.2:g.139346978T>C	GRCh38
NC_000003.11:g.139065820T>C , CM000665.1:g.139065820T>C	GRCh37
NC_000003.10:g.140548510T>C	NCBI36
NG_012174.1:g.7960T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478464.6:c.63T>C	ENSP00000419303.2:p.Phe21=
ENST00000480644.2:c.273T>C	ENSP00000420229.2:p.Phe91=
ENST00000492644.2:n.287T>C
ENST00000684961.1:c.-42-1182T>C	ENSP00000508439.1:n.-42-1182T>C
ENST00000686433.1:c.273T>C	ENSP00000509173.1:p.Phe91=
ENST00000687538.1:c.63T>C	ENSP00000508887.1:p.Phe21=
ENST00000688697.1:c.273T>C	ENSP00000510396.1:p.Phe91=
ENST00000689286.1:c.63T>C	ENSP00000509897.1:p.Phe21=
ENST00000689925.1:c.63T>C	ENSP00000510082.1:p.Phe21=
ENST00000690298.1:c.173-1182T>C	ENSP00000509376.1:n.173-1182T>C
ENST00000691070.1:c.273T>C	ENSP00000509723.1:p.Phe91=
ENST00000692727.1:n.287T>C
ENST00000693155.1:n.296T>C
ENST00000310776.9:c.270T>C	ENSP00000310785.5:p.Phe90=
ENST00000680020.1:c.273T>C MANE Select	ENSP00000505414.1:p.Phe91=
ENST00000310776.8:c.273T>C	ENSP00000310785.4:p.Phe91=
ENST00000465056.5:c.270T>C	ENSP00000418233.1:p.Phe90=
ENST00000465373.5:c.288T>C	ENSP00000419920.1:p.Phe96=
ENST00000466690.5:c.259T>C
ENST00000478464.5:c.150T>C	ENSP00000419303.1:p.Phe50=
ENST00000480938.5:n.273T>C
ENST00000483545.1:n.13T>C
ENST00000486705.1:n.184T>C
ENST00000495075.5:c.273T>C	ENSP00000418008.1:p.Phe91=
ENST00000498505.5:c.270T>C	ENSP00000420482.1:p.Phe90=
NM_020191.2:c.273T>C	NP_064576.1:p.Phe91=
XM_005247640.2:c.270T>C	XP_005247697.1:p.Phe90=
XM_006713703.2:c.273T>C	XP_006713766.1:p.Phe91=
XM_011512995.1:c.150T>C	XP_011511297.1:p.Phe50=
XM_011512996.1:c.147T>C	XP_011511298.1:p.Phe49=
NM_001363857.1:c.150T>C	NP_001350786.1:p.Phe50=
NM_001363893.1:c.270T>C	NP_001350822.1:p.Phe90=
NM_020191.3:c.273T>C	NP_064576.1:p.Phe91=
XM_006713703.4:c.273T>C	XP_006713766.1:p.Phe91=
XM_011512996.2:c.147T>C	XP_011511298.1:p.Phe49=
NM_020191.4:c.273T>C MANE Select	NP_064576.1:p.Phe91=