Canonical Allele Identifier: CA2335270779
Gene: SARS2 HGNC NCBI
MRPS12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930730C= , CM000681.2:g.38930730C= GRCh38
NC_000019.9:g.39421370C= , CM000681.1:g.39421370C= GRCh37
NC_000019.8:g.44113210C= NCBI36
NG_029222.1:g.5023C=
NG_031865.1:g.5167G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.11:c.7G= (SARS2) MANE Select ENSP00000221431.6:p.Ala3=
ENST00000221431.10:c.7G= (SARS2) ENSP00000221431.5:p.Ala3=
ENST00000308018.8:c.-288C= (MRPS12) ENSP00000308845.3:n.-288C=
ENST00000430193.7:c.7G= (SARS2) ENSP00000406754.3:p.Ala3=
ENST00000455102.6:c.7G= (SARS2) ENSP00000414954.2:p.Ala3=
ENST00000593754.1:c.7G= (SARS2) ENSP00000471767.1:p.Ala3=
ENST00000598343.5:c.7G= (SARS2) ENSP00000472576.1:p.Ala3=
ENST00000598598.5:n.34G= (SARS2)
ENST00000599996.1:c.476-4430G=
ENST00000600042.5:c.7G= (SARS2) ENSP00000472847.1:p.Ala3=
NM_001145901.1:c.7G= (SARS2) NP_001139373.1:p.Ala3=
NM_017827.3:c.7G= (SARS2) NP_060297.1:p.Ala3=
NM_033362.3:c.-288C= (MRPS12) NP_203526.1:n.-288C=
NM_001145901.2:c.7G= (SARS2) NP_001139373.1:p.Ala3=
NM_017827.4:c.7G= (SARS2) MANE Select NP_060297.1:p.Ala3=