Canonical Allele Identifier: CA995758159

Gene: SARS2

Linked Data

• dbSNP Id: rs1974715804
• gnomAD v3: 19-38930446-C-CCCGG
• gnomAD v4: 19-38930446-C-CCCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.38930452_38930455dup , CM000681.2:g.38930452_38930455dup	GRCh38
NC_000019.9:g.39421092_39421095dup , CM000681.1:g.39421092_39421095dup	GRCh37
NC_000019.8:g.44112932_44112935dup	NCBI36
NG_029222.1:g.4745_4748dup
NG_031865.1:g.5447_5450dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221431.11:c.267+20_267+23dup MANE Select	ENSP00000221431.6:n.267+20_267+23dup
ENST00000221431.10:c.267+20_267+23dup	ENSP00000221431.5:n.267+20_267+23dup
ENST00000430193.7:c.267+20_267+23dup	ENSP00000406754.3:n.267+20_267+23dup
ENST00000455102.6:c.267+20_267+23dup	ENSP00000414954.2:n.267+20_267+23dup
ENST00000593754.1:c.267+20_267+23dup	ENSP00000471767.1:n.267+20_267+23dup
ENST00000598343.5:c.267+20_267+23dup	ENSP00000472576.1:n.267+20_267+23dup
ENST00000598598.5:n.294+20_294+23dup
ENST00000599996.1:c.476-4150_476-4147dup
ENST00000600042.5:c.267+20_267+23dup	ENSP00000472847.1:n.267+20_267+23dup
NM_001145901.1:c.267+20_267+23dup	NP_001139373.1:n.267+20_267+23dup
NM_017827.3:c.267+20_267+23dup	NP_060297.1:n.267+20_267+23dup
NM_001145901.2:c.267+20_267+23dup	NP_001139373.1:n.267+20_267+23dup
NM_017827.4:c.267+20_267+23dup MANE Select	NP_060297.1:n.267+20_267+23dup