Canonical Allele Identifier: CA2335270733
Gene: SARS2 HGNC NCBI
MRPS12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930645C= , CM000681.2:g.38930645C= GRCh38
NC_000019.9:g.39421285C= , CM000681.1:g.39421285C= GRCh37
NC_000019.8:g.44113125C= NCBI36
NG_029222.1:g.4938C=
NG_031865.1:g.5252G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.11:c.92G= (SARS2) MANE Select ENSP00000221431.6:p.Arg31=
ENST00000221431.10:c.92G= (SARS2) ENSP00000221431.5:p.Arg31=
ENST00000308018.8:c.-373C= (MRPS12) ENSP00000308845.3:n.-373C=
ENST00000430193.7:c.92G= (SARS2) ENSP00000406754.3:p.Arg31=
ENST00000455102.6:c.92G= (SARS2) ENSP00000414954.2:p.Arg31=
ENST00000593754.1:c.92G= (SARS2) ENSP00000471767.1:p.Arg31=
ENST00000598343.5:c.92G= (SARS2) ENSP00000472576.1:p.Arg31=
ENST00000598598.5:n.119G= (SARS2)
ENST00000599996.1:c.476-4345G=
ENST00000600042.5:c.92G= (SARS2) ENSP00000472847.1:p.Arg31=
NM_001145901.1:c.92G= (SARS2) NP_001139373.1:p.Arg31=
NM_017827.3:c.92G= (SARS2) NP_060297.1:p.Arg31=
NM_001145901.2:c.92G= (SARS2) NP_001139373.1:p.Arg31=
NM_017827.4:c.92G= (SARS2) MANE Select NP_060297.1:p.Arg31=