Canonical Allele Identifier: CA354763031

Gene: MRPS22

Linked Data

• MyVariant Identifiers: chr3:g.139071533T>G (hg19) ; chr3:g.139352691T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.139352691T>G , CM000665.2:g.139352691T>G	GRCh38
NC_000003.11:g.139071533T>G , CM000665.1:g.139071533T>G	GRCh37
NC_000003.10:g.140554223T>G	NCBI36
NG_012174.1:g.13673T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000478464.6:c.567T>G	ENSP00000419303.2:p.Tyr189Ter
ENST00000480644.2:c.693T>G	ENSP00000420229.2:p.Tyr231Ter
ENST00000492644.2:n.3031T>G
ENST00000684961.1:c.396T>G	ENSP00000508439.1:p.Tyr132Ter
ENST00000686433.1:c.723T>G	ENSP00000509173.1:p.Tyr241Ter
ENST00000687538.1:c.567T>G	ENSP00000508887.1:p.Tyr189Ter
ENST00000688697.1:c.777T>G	ENSP00000510396.1:p.Tyr259Ter
ENST00000689286.1:c.567T>G	ENSP00000509897.1:p.Tyr189Ter
ENST00000689925.1:c.*118T>G	ENSP00000510082.1:n.*118T>G
ENST00000690298.1:c.*418T>G	ENSP00000509376.1:n.*418T>G
ENST00000691070.1:c.693T>G	ENSP00000509723.1:p.Tyr231Ter
ENST00000692727.1:n.3299T>G
ENST00000693155.1:n.1454T>G
ENST00000310776.9:c.774T>G	ENSP00000310785.5:p.Tyr258Ter
ENST00000680020.1:c.777T>G MANE Select	ENSP00000505414.1:p.Tyr259Ter
ENST00000310776.8:c.777T>G	ENSP00000310785.4:p.Tyr259Ter
ENST00000465056.5:c.774T>G	ENSP00000418233.1:p.Tyr258Ter
ENST00000478464.5:c.654T>G	ENSP00000419303.1:p.Tyr218Ter
ENST00000480644.1:c.262T>G
ENST00000480938.5:n.1431T>G
ENST00000492644.1:n.1822T>G
ENST00000495075.5:c.777T>G	ENSP00000418008.1:p.Tyr259Ter
ENST00000498505.5:c.*374T>G	ENSP00000420482.1:n.*374T>G
NM_020191.2:c.777T>G	NP_064576.1:p.Tyr259Ter
XM_005247640.2:c.774T>G	XP_005247697.1:p.Tyr258Ter
XM_006713703.2:c.723T>G	XP_006713766.1:p.Tyr241Ter
XM_011512995.1:c.654T>G	XP_011511297.1:p.Tyr218Ter
XM_011512996.1:c.651T>G	XP_011511298.1:p.Tyr217Ter
NM_001363857.1:c.654T>G	NP_001350786.1:p.Tyr218Ter
NM_001363893.1:c.774T>G	NP_001350822.1:p.Tyr258Ter
NM_020191.3:c.777T>G	NP_064576.1:p.Tyr259Ter
XM_006713703.4:c.723T>G	XP_006713766.1:p.Tyr241Ter
XM_011512996.2:c.651T>G	XP_011511298.1:p.Tyr217Ter
NM_020191.4:c.777T>G MANE Select	NP_064576.1:p.Tyr259Ter