Canonical Allele Identifier: CA2335270590
Gene: SARS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38930422_38930423delinsTC , CM000681.2:g.38930422_38930423delinsTC GRCh38
NC_000019.9:g.39421062_39421063delinsTC , CM000681.1:g.39421062_39421063delinsTC GRCh37
NC_000019.8:g.44112902_44112903delinsTC NCBI36
NG_029222.1:g.4715_4716delinsTC
NG_031865.1:g.5474_5475delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000221431.11:c.267+47_267+48delinsGA MANE Select ENSP00000221431.6:n.267+47_267+48delinsGA
ENST00000221431.10:c.267+47_267+48delinsGA ENSP00000221431.5:n.267+47_267+48delinsGA
ENST00000430193.7:c.267+47_267+48delinsGA ENSP00000406754.3:n.267+47_267+48delinsGA
ENST00000455102.6:c.267+47_267+48delinsGA ENSP00000414954.2:n.267+47_267+48delinsGA
ENST00000593754.1:c.267+47_267+48delinsGA ENSP00000471767.1:n.267+47_267+48delinsGA
ENST00000598343.5:c.267+47_267+48delinsGA ENSP00000472576.1:n.267+47_267+48delinsGA
ENST00000598598.5:n.294+47_294+48delinsGA
ENST00000599996.1:c.476-4123_476-4122delinsGA
ENST00000600042.5:c.267+47_267+48delinsGA ENSP00000472847.1:n.267+47_267+48delinsGA
NM_001145901.1:c.267+47_267+48delinsGA NP_001139373.1:n.267+47_267+48delinsGA
NM_017827.3:c.267+47_267+48delinsGA NP_060297.1:n.267+47_267+48delinsGA
NM_001145901.2:c.267+47_267+48delinsGA NP_001139373.1:n.267+47_267+48delinsGA
NM_017827.4:c.267+47_267+48delinsGA MANE Select NP_060297.1:n.267+47_267+48delinsGA