Canonical Allele Identifier: CA1240426702
Gene: MRPL33 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.27772914A>T , CM000664.2:g.27772914A>T GRCh38
NC_000002.11:g.27995781A>T , CM000664.1:g.27995781A>T GRCh37
NC_000002.10:g.27849285A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296102.8:c.41+222A>T MANE Select ENSP00000296102.3:n.41+222A>T
ENST00000296102.7:c.41+222A>T ENSP00000296102.3:n.41+222A>T
ENST00000379666.7:c.41+222A>T ENSP00000368988.3:n.41+222A>T
ENST00000448427.1:c.41+222A>T ENSP00000407385.1:n.41+222A>T
ENST00000476552.1:n.215+222A>T
ENST00000483992.5:n.430+222A>T
NM_004891.3:c.41+222A>T NP_004882.1:n.41+222A>T
NM_145330.2:c.41+222A>T NP_663303.1:n.41+222A>T
NM_004891.4:c.41+222A>T MANE Select NP_004882.1:n.41+222A>T
NM_145330.3:c.41+222A>T NP_663303.1:n.41+222A>T