Canonical Allele Identifier: CA2389091565

Gene: ETS2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823877_38823879delinsCTG , CM000683.2:g.38823877_38823879delinsCTG	GRCh38
NC_000021.8:g.40195801_40195803delinsCTG , CM000683.1:g.40195801_40195803delinsCTG	GRCh37
NC_000021.7:g.39117671_39117673delinsCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.*988_*990delinsCTG	ENSP00000353344.3:n.*988_*990delinsCTG
ENST00000360938.8:c.*988_*990delinsCTG MANE Select	ENSP00000354194.3:n.*988_*990delinsCTG
ENST00000653642.1:c.*988_*990delinsCTG	ENSP00000499315.1:n.*988_*990delinsCTG
ENST00000666778.1:c.*988_*990delinsCTG	ENSP00000499775.1:n.*988_*990delinsCTG
ENST00000667466.1:c.*988_*990delinsCTG	ENSP00000499540.1:n.*988_*990delinsCTG
ENST00000360214.7:c.*988_*990delinsCTG	ENSP00000353344.3:n.*988_*990delinsCTG
ENST00000360938.7:c.*988_*990delinsCTG	ENSP00000354194.3:n.*988_*990delinsCTG
NM_001256295.1:c.*988_*990delinsCTG	NP_001243224.1:n.*988_*990delinsCTG
NM_005239.5:c.*988_*990delinsCTG	NP_005230.1:n.*988_*990delinsCTG
XM_005260935.1:c.*988_*990delinsCTG	XP_005260992.1:n.*988_*990delinsCTG
XM_017028290.1:c.*988_*990delinsCTG	XP_016883779.1:n.*988_*990delinsCTG
NM_005239.6:c.*988_*990delinsCTG MANE Select	NP_005230.1:n.*988_*990delinsCTG
NM_001256295.2:c.*988_*990delinsCTG	NP_001243224.1:n.*988_*990delinsCTG