Canonical Allele Identifier: CA1022324176

Gene: ETS2

Linked Data

• dbSNP Id: rs1986308228
• gnomAD v3: 21-38823386-C-CAGTT
• gnomAD v4: 21-38823386-C-CAGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823387_38823390dup , CM000683.2:g.38823387_38823390dup	GRCh38
NC_000021.8:g.40195311_40195314dup , CM000683.1:g.40195311_40195314dup	GRCh37
NC_000021.7:g.39117181_39117184dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*498_*501dup	ENSP00000353344.3:n.*498_*501dup
ENST00000360938.8:c.*498_*501dup MANE Select	ENSP00000354194.3:n.*498_*501dup
ENST00000653642.1:c.*498_*501dup	ENSP00000499315.1:n.*498_*501dup
ENST00000662305.1:c.*498_*501dup	ENSP00000499226.1:n.*498_*501dup
ENST00000666778.1:c.*498_*501dup	ENSP00000499775.1:n.*498_*501dup
ENST00000667466.1:c.*498_*501dup	ENSP00000499540.1:n.*498_*501dup
ENST00000360214.7:c.*498_*501dup	ENSP00000353344.3:n.*498_*501dup
ENST00000360938.7:c.*498_*501dup	ENSP00000354194.3:n.*498_*501dup
NM_001256295.1:c.*498_*501dup	NP_001243224.1:n.*498_*501dup
NM_005239.5:c.*498_*501dup	NP_005230.1:n.*498_*501dup
XM_005260935.1:c.*498_*501dup	XP_005260992.1:n.*498_*501dup
XM_017028290.1:c.*498_*501dup	XP_016883779.1:n.*498_*501dup
NM_005239.6:c.*498_*501dup MANE Select	NP_005230.1:n.*498_*501dup
NM_001256295.2:c.*498_*501dup	NP_001243224.1:n.*498_*501dup