Canonical Allele Identifier: CA7890329
Community Standard Title: NM_019109.5(ALG1):c.1292C>T (p.Ala431Val)
Gene: ALG1 HGNC NCBI
EEF2KMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.5084778C>T , CM000678.2:g.5084778C>T GRCh38
NC_000016.9:g.5134779C>T , CM000678.1:g.5134779C>T GRCh37
NC_000016.8:g.5074780C>T NCBI36
NG_009202.1:g.17970C>T

Transcript Alleles

HGVS Amino-acid Change
NM_019109.5:c.1292C>T (ALG1) MANE Select NP_061982.3:p.Ala431Val
NM_201400.4:c.*854G>A (EEF2KMT) MANE Select NP_958802.1:n.*854G>A
ENST00000262374.10:c.1292C>T (ALG1) MANE Select ENSP00000262374.5:p.Ala431Val
ENST00000427587.9:c.*854G>A (EEF2KMT) MANE Select ENSP00000398502.3:n.*854G>A
NM_001289029.1:c.*854G>A (EEF2KMT) NP_001275958.1:n.*854G>A
NM_001289029.2:c.*854G>A (EEF2KMT) NP_001275958.1:n.*854G>A
NM_001330504.1:c.959C>T (ALG1) NP_001317433.1:p.Ala320Val
NM_001330504.2:c.959C>T (ALG1) NP_001317433.1:p.Ala320Val
NM_019109.4:c.1292C>T (ALG1) NP_061982.3:p.Ala431Val
NM_201400.3:c.*854G>A (EEF2KMT) NP_958802.1:n.*854G>A
NM_201598.3:c.*854G>A (EEF2KMT) NP_963892.1:n.*854G>A
NM_201598.4:c.*854G>A (EEF2KMT) NP_963892.1:n.*854G>A
ENST00000262374.9:c.1292C>T (ALG1) ENSP00000262374.4:p.Ala431Val
ENST00000427587.8:c.*854G>A (EEF2KMT) ENSP00000398502.3:n.*854G>A
ENST00000458008.8:c.*854G>A (EEF2KMT) ENSP00000389710.3:n.*854G>A
ENST00000544428.1:c.959C>T (ALG1) ENSP00000440019.1:p.Ala320Val
ENST00000585436.5:c.*1355G>A (EEF2KMT) ENSP00000464781.1:n.*1355G>A
ENST00000588623.5:c.959C>T (ALG1) ENSP00000468118.1:p.Ala320Val
ENST00000591822.5:c.*1193C>T (ALG1) ENSP00000467865.1:n.*1193C>T
ENST00000592793.6:n.3428C>T (ALG1)
ENST00000650085.1:n.2116C>T (ALG1)
ENST00000682020.1:c.698C>T (ALG1) ENSP00000508075.1:p.Ala233Val
ENST00000682206.1:c.*387C>T (ALG1) ENSP00000508285.1:n.*387C>T
ENST00000682314.1:n.2348C>T (ALG1)
ENST00000682327.1:c.764C>T (ALG1) ENSP00000507058.1:p.Ala255Val
ENST00000682349.1:n.3434C>T (ALG1)
ENST00000682703.1:n.5268C>T (ALG1)
ENST00000682797.1:c.*384C>T (ALG1) ENSP00000507582.1:n.*384C>T
ENST00000682985.1:c.803C>T (ALG1) ENSP00000507598.1:p.Ala268Val
ENST00000683433.1:c.551C>T (ALG1) ENSP00000507463.1:p.Ala184Val
ENST00000683685.1:n.3174C>T (ALG1)
ENST00000683710.1:c.*1259C>T (ALG1) ENSP00000506785.1:n.*1259C>T
ENST00000683739.1:c.959C>T (ALG1) ENSP00000507002.1:p.Ala320Val
ENST00000683772.1:n.2344C>T (ALG1)
ENST00000684008.1:c.1230C>T (ALG1) ENSP00000507962.1:n.1230C>T
ENST00000684190.1:c.1253C>T (ALG1) ENSP00000507554.1:p.Ala418Val
ENST00000684335.1:c.1181C>T (ALG1) ENSP00000508112.1:p.Ala394Val
XM_005255157.4:c.*854G>A (EEF2KMT) XP_005255214.1:n.*854G>A
XM_005255158.4:c.*854G>A (EEF2KMT) XP_005255215.1:n.*854G>A
XM_011522404.2:c.*854G>A (EEF2KMT) XP_011520706.1:n.*854G>A
XM_011522565.1:c.959C>T (ALG1) XP_011520867.1:p.Ala320Val
XM_017023457.2:c.1253C>T (ALG1) XP_016878946.1:p.Ala418Val
XM_017023458.1:c.959C>T (ALG1) XP_016878947.1:p.Ala320Val
XR_932882.3:n.1321C>T (ALG1)