Canonical Allele Identifier: CA920306103

Gene: ETS2

Linked Data

• dbSNP Id: rs11422952
• gnomAD v3: 21-38823617-GTTTT-G
• gnomAD v4: 21-38823617-GTTTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823621_38823624del , CM000683.2:g.38823621_38823624del	GRCh38
NC_000021.8:g.40195545_40195548del , CM000683.1:g.40195545_40195548del	GRCh37
NC_000021.7:g.39117415_39117418del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*732_*735del	ENSP00000353344.3:n.*732_*735del
ENST00000360938.8:c.*732_*735del MANE Select	ENSP00000354194.3:n.*732_*735del
ENST00000653642.1:c.*732_*735del	ENSP00000499315.1:n.*732_*735del
ENST00000662305.1:c.*732_*735del	ENSP00000499226.1:n.*732_*735del
ENST00000666778.1:c.*732_*735del	ENSP00000499775.1:n.*732_*735del
ENST00000667466.1:c.*732_*735del	ENSP00000499540.1:n.*732_*735del
ENST00000360214.7:c.*732_*735del	ENSP00000353344.3:n.*732_*735del
ENST00000360938.7:c.*732_*735del	ENSP00000354194.3:n.*732_*735del
NM_001256295.1:c.*732_*735del	NP_001243224.1:n.*732_*735del
NM_005239.5:c.*732_*735del	NP_005230.1:n.*732_*735del
XM_005260935.1:c.*732_*735del	XP_005260992.1:n.*732_*735del
XM_017028290.1:c.*732_*735del	XP_016883779.1:n.*732_*735del
NM_005239.6:c.*732_*735del MANE Select	NP_005230.1:n.*732_*735del
NM_001256295.2:c.*732_*735del	NP_001243224.1:n.*732_*735del