Canonical Allele Identifier: CA2335270629
Gene: SARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930472T= , CM000681.2:g.38930472T= GRCh38
NC_000019.9:g.39421112T= , CM000681.1:g.39421112T= GRCh37
NC_000019.8:g.44112952T= NCBI36
NG_029222.1:g.4765T=
NG_031865.1:g.5425A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.11:c.265A= MANE Select ENSP00000221431.6:p.Ile89=
ENST00000221431.10:c.265A= ENSP00000221431.5:p.Ile89=
ENST00000430193.7:c.265A= ENSP00000406754.3:p.Ile89=
ENST00000455102.6:c.265A= ENSP00000414954.2:p.Ile89=
ENST00000593754.1:c.265A= ENSP00000471767.1:p.Ile89=
ENST00000598343.5:c.265A= ENSP00000472576.1:p.Ile89=
ENST00000598598.5:n.292A=
ENST00000599996.1:c.476-4172A=
ENST00000600042.5:c.265A= ENSP00000472847.1:p.Ile89=
NM_001145901.1:c.265A= NP_001139373.1:p.Ile89=
NM_017827.3:c.265A= NP_060297.1:p.Ile89=
NM_001145901.2:c.265A= NP_001139373.1:p.Ile89=
NM_017827.4:c.265A= MANE Select NP_060297.1:p.Ile89=