Canonical Allele Identifier: CA1405584384

Gene: MRPS22

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.139350183G= , CM000665.2:g.139350183G=	GRCh38
NC_000003.11:g.139069025G= , CM000665.1:g.139069025G=	GRCh37
NC_000003.10:g.140551715G=	NCBI36
NG_012174.1:g.11165G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000478464.6:c.299G=	ENSP00000419303.2:p.Arg100=
ENST00000480644.2:c.509G=	ENSP00000420229.2:p.Arg170=
ENST00000492644.2:n.523G=
ENST00000684961.1:c.128G=	ENSP00000508439.1:p.Arg43=
ENST00000686433.1:c.509G=	ENSP00000509173.1:p.Arg170=
ENST00000687538.1:c.299G=	ENSP00000508887.1:p.Arg100=
ENST00000688697.1:c.509G=	ENSP00000510396.1:p.Arg170=
ENST00000689286.1:c.299G=	ENSP00000509897.1:p.Arg100=
ENST00000689925.1:c.299G=	ENSP00000510082.1:p.Arg100=
ENST00000690298.1:c.*150G=	ENSP00000509376.1:n.*150G=
ENST00000691070.1:c.509G=	ENSP00000509723.1:p.Arg170=
ENST00000692727.1:n.2377G=
ENST00000693155.1:n.532G=
ENST00000310776.9:c.506G=	ENSP00000310785.5:p.Arg169=
ENST00000680020.1:c.509G= MANE Select	ENSP00000505414.1:p.Arg170=
ENST00000310776.8:c.509G=	ENSP00000310785.4:p.Arg170=
ENST00000465056.5:c.506G=	ENSP00000418233.1:p.Arg169=
ENST00000465373.5:c.524G=	ENSP00000419920.1:p.Arg175=
ENST00000466690.5:c.602G=
ENST00000478464.5:c.386G=	ENSP00000419303.1:p.Arg129=
ENST00000480644.1:c.48G=
ENST00000480938.5:n.509G=
ENST00000483545.1:n.249G=
ENST00000495075.5:c.509G=	ENSP00000418008.1:p.Arg170=
ENST00000498505.5:c.*106G=	ENSP00000420482.1:n.*106G=
NM_020191.2:c.509G=	NP_064576.1:p.Arg170=
XM_005247640.2:c.506G=	XP_005247697.1:p.Arg169=
XM_006713703.2:c.509G=	XP_006713766.1:p.Arg170=
XM_011512995.1:c.386G=	XP_011511297.1:p.Arg129=
XM_011512996.1:c.383G=	XP_011511298.1:p.Arg128=
NM_001363857.1:c.386G=	NP_001350786.1:p.Arg129=
NM_001363893.1:c.506G=	NP_001350822.1:p.Arg169=
NM_020191.3:c.509G=	NP_064576.1:p.Arg170=
XM_006713703.4:c.509G=	XP_006713766.1:p.Arg170=
XM_011512996.2:c.383G=	XP_011511298.1:p.Arg128=
NM_020191.4:c.509G= MANE Select	NP_064576.1:p.Arg170=