Canonical Allele Identifier: CA637810284

Gene: ETS2

Linked Data

• dbSNP Id: rs1189957453
• gnomAD v2: 21-40195346-A-AAAT
• gnomAD v3: 21-38823422-A-AAAT
• gnomAD v4: 21-38823422-A-AAAT
• MyVariant Identifiers: chr21:g.40195346_40195347insAAT (hg19) ; chr21:g.38823422_38823423insAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823426_38823428dup , CM000683.2:g.38823426_38823428dup	GRCh38
NC_000021.8:g.40195350_40195352dup , CM000683.1:g.40195350_40195352dup	GRCh37
NC_000021.7:g.39117220_39117222dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*537_*539dup	ENSP00000353344.3:n.*537_*539dup
ENST00000360938.8:c.*537_*539dup MANE Select	ENSP00000354194.3:n.*537_*539dup
ENST00000653642.1:c.*537_*539dup	ENSP00000499315.1:n.*537_*539dup
ENST00000662305.1:c.*537_*539dup	ENSP00000499226.1:n.*537_*539dup
ENST00000666778.1:c.*537_*539dup	ENSP00000499775.1:n.*537_*539dup
ENST00000667466.1:c.*537_*539dup	ENSP00000499540.1:n.*537_*539dup
ENST00000360214.7:c.*537_*539dup	ENSP00000353344.3:n.*537_*539dup
ENST00000360938.7:c.*537_*539dup	ENSP00000354194.3:n.*537_*539dup
NM_001256295.1:c.*537_*539dup	NP_001243224.1:n.*537_*539dup
NM_005239.5:c.*537_*539dup	NP_005230.1:n.*537_*539dup
XM_005260935.1:c.*537_*539dup	XP_005260992.1:n.*537_*539dup
XM_017028290.1:c.*537_*539dup	XP_016883779.1:n.*537_*539dup
NM_005239.6:c.*537_*539dup MANE Select	NP_005230.1:n.*537_*539dup
NM_001256295.2:c.*537_*539dup	NP_001243224.1:n.*537_*539dup