Canonical Allele Identifier: CA2335270695

Gene: SARS2 MRPS12

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930567T= , CM000681.2:g.38930567T=	GRCh38
NC_000019.9:g.39421207T= , CM000681.1:g.39421207T=	GRCh37
NC_000019.8:g.44113047T=	NCBI36
NG_029222.1:g.4860T=
NG_031865.1:g.5330A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.170A= (SARS2) MANE Select	ENSP00000221431.6:p.Gln57=
ENST00000221431.10:c.170A= (SARS2)	ENSP00000221431.5:p.Gln57=
ENST00000308018.8:c.-451T= (MRPS12)	ENSP00000308845.3:n.-451T=
ENST00000430193.7:c.170A= (SARS2)	ENSP00000406754.3:p.Gln57=
ENST00000455102.6:c.170A= (SARS2)	ENSP00000414954.2:p.Gln57=
ENST00000593754.1:c.170A= (SARS2)	ENSP00000471767.1:p.Gln57=
ENST00000598343.5:c.170A= (SARS2)	ENSP00000472576.1:p.Gln57=
ENST00000598598.5:n.197A= (SARS2)
ENST00000599996.1:c.476-4267A=
ENST00000600042.5:c.170A= (SARS2)	ENSP00000472847.1:p.Gln57=
NM_001145901.1:c.170A= (SARS2)	NP_001139373.1:p.Gln57=
NM_017827.3:c.170A= (SARS2)	NP_060297.1:p.Gln57=
NM_001145901.2:c.170A= (SARS2)	NP_001139373.1:p.Gln57=
NM_017827.4:c.170A= (SARS2) MANE Select	NP_060297.1:p.Gln57=