Canonical Allele Identifier: CA2389091476

Gene: ETS2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823637_38823638delinsGT , CM000683.2:g.38823637_38823638delinsGT	GRCh38
NC_000021.8:g.40195561_40195562delinsGT , CM000683.1:g.40195561_40195562delinsGT	GRCh37
NC_000021.7:g.39117431_39117432delinsGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*748_*749delinsGT	ENSP00000353344.3:n.*748_*749delinsGT
ENST00000360938.8:c.*748_*749delinsGT MANE Select	ENSP00000354194.3:n.*748_*749delinsGT
ENST00000653642.1:c.*748_*749delinsGT	ENSP00000499315.1:n.*748_*749delinsGT
ENST00000662305.1:c.*748_*749delinsGT	ENSP00000499226.1:n.*748_*749delinsGT
ENST00000666778.1:c.*748_*749delinsGT	ENSP00000499775.1:n.*748_*749delinsGT
ENST00000667466.1:c.*748_*749delinsGT	ENSP00000499540.1:n.*748_*749delinsGT
ENST00000360214.7:c.*748_*749delinsGT	ENSP00000353344.3:n.*748_*749delinsGT
ENST00000360938.7:c.*748_*749delinsGT	ENSP00000354194.3:n.*748_*749delinsGT
NM_001256295.1:c.*748_*749delinsGT	NP_001243224.1:n.*748_*749delinsGT
NM_005239.5:c.*748_*749delinsGT	NP_005230.1:n.*748_*749delinsGT
XM_005260935.1:c.*748_*749delinsGT	XP_005260992.1:n.*748_*749delinsGT
XM_017028290.1:c.*748_*749delinsGT	XP_016883779.1:n.*748_*749delinsGT
NM_005239.6:c.*748_*749delinsGT MANE Select	NP_005230.1:n.*748_*749delinsGT
NM_001256295.2:c.*748_*749delinsGT	NP_001243224.1:n.*748_*749delinsGT