Canonical Allele Identifier: CA405742621

Gene: SARS2 MRPS12

Linked Data

• COSMIC: COSM6424827 ; COSM6424828
• MyVariant Identifiers: chr19:g.39421349A>G (hg19) ; chr19:g.38930709A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930709A>G , CM000681.2:g.38930709A>G	GRCh38
NC_000019.9:g.39421349A>G , CM000681.1:g.39421349A>G	GRCh37
NC_000019.8:g.44113189A>G	NCBI36
NG_029222.1:g.5002A>G
NG_031865.1:g.5188T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.28T>C (SARS2) MANE Select	ENSP00000221431.6:p.Trp10Arg
ENST00000221431.10:c.28T>C (SARS2)	ENSP00000221431.5:p.Trp10Arg
ENST00000308018.8:c.-309A>G (MRPS12)	ENSP00000308845.3:n.-309A>G
ENST00000430193.7:c.28T>C (SARS2)	ENSP00000406754.3:p.Trp10Arg
ENST00000455102.6:c.28T>C (SARS2)	ENSP00000414954.2:p.Trp10Arg
ENST00000593754.1:c.28T>C (SARS2)	ENSP00000471767.1:p.Trp10Arg
ENST00000598343.5:c.28T>C (SARS2)	ENSP00000472576.1:p.Trp10Arg
ENST00000598598.5:n.55T>C (SARS2)
ENST00000599996.1:c.476-4409T>C
ENST00000600042.5:c.28T>C (SARS2)	ENSP00000472847.1:p.Trp10Arg
NM_001145901.1:c.28T>C (SARS2)	NP_001139373.1:p.Trp10Arg
NM_017827.3:c.28T>C (SARS2)	NP_060297.1:p.Trp10Arg
NM_033362.3:c.-309A>G (MRPS12)	NP_203526.1:n.-309A>G
NM_001145901.2:c.28T>C (SARS2)	NP_001139373.1:p.Trp10Arg
NM_017827.4:c.28T>C (SARS2) MANE Select	NP_060297.1:p.Trp10Arg