Canonical Allele Identifier: CA2335270777
Gene: SARS2 HGNC NCBI
MRPS12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930726G= , CM000681.2:g.38930726G= GRCh38
NC_000019.9:g.39421366G= , CM000681.1:g.39421366G= GRCh37
NC_000019.8:g.44113206G= NCBI36
NG_029222.1:g.5019G=
NG_031865.1:g.5171C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.11:c.11C= (SARS2) MANE Select ENSP00000221431.6:p.Ser4=
ENST00000221431.10:c.11C= (SARS2) ENSP00000221431.5:p.Ser4=
ENST00000308018.8:c.-292G= (MRPS12) ENSP00000308845.3:n.-292G=
ENST00000430193.7:c.11C= (SARS2) ENSP00000406754.3:p.Ser4=
ENST00000455102.6:c.11C= (SARS2) ENSP00000414954.2:p.Ser4=
ENST00000593754.1:c.11C= (SARS2) ENSP00000471767.1:p.Ser4=
ENST00000598343.5:c.11C= (SARS2) ENSP00000472576.1:p.Ser4=
ENST00000598598.5:n.38C= (SARS2)
ENST00000599996.1:c.476-4426C=
ENST00000600042.5:c.11C= (SARS2) ENSP00000472847.1:p.Ser4=
NM_001145901.1:c.11C= (SARS2) NP_001139373.1:p.Ser4=
NM_017827.3:c.11C= (SARS2) NP_060297.1:p.Ser4=
NM_033362.3:c.-292G= (MRPS12) NP_203526.1:n.-292G=
NM_001145901.2:c.11C= (SARS2) NP_001139373.1:p.Ser4=
NM_017827.4:c.11C= (SARS2) MANE Select NP_060297.1:p.Ser4=