Canonical Allele Identifier: CA1883732979

Gene: MRPS2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.135503655G= , CM000671.2:g.135503655G=	GRCh38
NC_000009.11:g.138395501G= , CM000671.1:g.138395501G=	GRCh37
NC_000009.10:g.137535322G=	NCBI36
NG_042313.1:g.8025G=

Transcript Alleles

HGVS	Amino-acid Change
NM_016034.5:c.413G= MANE Select	NP_057118.1:p.Arg138=
ENST00000241600.10:c.413G= MANE Select	ENSP00000241600.5:p.Arg138=
NM_001371401.1:c.413G=	NP_001358330.1:p.Arg138=
NM_016034.4:c.413G=	NP_057118.1:p.Arg138=
NR_051967.1:n.636G=
NR_051967.3:n.585G=
NR_051968.1:n.691G=
NR_051968.2:n.640G=
NR_051969.1:n.696G=
NR_051969.2:n.645G=
NR_051970.1:n.638G=
NR_051970.2:n.587G=
NR_121579.1:n.735C=
ENST00000241600.9:c.413G=	ENSP00000241600.5:p.Arg138=
ENST00000371785.5:c.413G=	ENSP00000360850.1:p.Arg138=
ENST00000453385.1:c.455G=	ENSP00000400082.1:p.Arg152=
ENST00000462948.6:c.*286G=	ENSP00000511903.1:n.*286G=
ENST00000472852.1:n.554G=
ENST00000472852.2:c.*219G=	ENSP00000511904.1:n.*219G=
ENST00000472946.1:n.164G=
ENST00000472946.2:n.178G=
ENST00000485333.5:n.560G=
ENST00000485333.6:c.*244G=	ENSP00000511905.1:n.*244G=
ENST00000488610.5:n.623G=
ENST00000488610.6:c.*302G=	ENSP00000511906.1:n.*302G=
XM_006717136.2:c.482G=	XP_006717199.1:p.Arg161=
XM_006717136.3:c.482G=	XP_006717199.1:p.Arg161=