Canonical Allele Identifier: CA2654516729

Gene: ETS2

Linked Data

• gnomAD v4: 21-38823848-CACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823850_38823852del , CM000683.2:g.38823850_38823852del	GRCh38
NC_000021.8:g.40195774_40195776del , CM000683.1:g.40195774_40195776del	GRCh37
NC_000021.7:g.39117644_39117646del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*961_*963del	ENSP00000353344.3:n.*961_*963del
ENST00000360938.8:c.*961_*963del MANE Select	ENSP00000354194.3:n.*961_*963del
ENST00000653642.1:c.*961_*963del	ENSP00000499315.1:n.*961_*963del
ENST00000666778.1:c.*961_*963del	ENSP00000499775.1:n.*961_*963del
ENST00000667466.1:c.*961_*963del	ENSP00000499540.1:n.*961_*963del
ENST00000360214.7:c.*961_*963del	ENSP00000353344.3:n.*961_*963del
ENST00000360938.7:c.*961_*963del	ENSP00000354194.3:n.*961_*963del
NM_001256295.1:c.*961_*963del	NP_001243224.1:n.*961_*963del
NM_005239.5:c.*961_*963del	NP_005230.1:n.*961_*963del
XM_005260935.1:c.*961_*963del	XP_005260992.1:n.*961_*963del
XM_017028290.1:c.*961_*963del	XP_016883779.1:n.*961_*963del
NM_005239.6:c.*961_*963del MANE Select	NP_005230.1:n.*961_*963del
NM_001256295.2:c.*961_*963del	NP_001243224.1:n.*961_*963del