Canonical Allele Identifier: CA637810350

Gene: ETS2

Linked Data

• dbSNP Id: rs1432681403
• gnomAD v2: 21-40195801-CTG-C
• gnomAD v3: 21-38823877-CTG-C
• gnomAD v4: 21-38823877-CTG-C
• MyVariant Identifiers: chr21:g.40195802_40195803del (hg19) ; chr21:g.38823878_38823879del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38823881_38823882del , CM000683.2:g.38823881_38823882del	GRCh38
NC_000021.8:g.40195805_40195806del , CM000683.1:g.40195805_40195806del	GRCh37
NC_000021.7:g.39117675_39117676del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360214.8:c.*992_*993del	ENSP00000353344.3:n.*992_*993del
ENST00000360938.8:c.*992_*993del MANE Select	ENSP00000354194.3:n.*992_*993del
ENST00000653642.1:c.*992_*993del	ENSP00000499315.1:n.*992_*993del
ENST00000666778.1:c.*992_*993del	ENSP00000499775.1:n.*992_*993del
ENST00000667466.1:c.*992_*993del	ENSP00000499540.1:n.*992_*993del
ENST00000360214.7:c.*992_*993del	ENSP00000353344.3:n.*992_*993del
ENST00000360938.7:c.*992_*993del	ENSP00000354194.3:n.*992_*993del
NM_001256295.1:c.*992_*993del	NP_001243224.1:n.*992_*993del
NM_005239.5:c.*992_*993del	NP_005230.1:n.*992_*993del
XM_005260935.1:c.*992_*993del	XP_005260992.1:n.*992_*993del
XM_017028290.1:c.*992_*993del	XP_016883779.1:n.*992_*993del
NM_005239.6:c.*992_*993del MANE Select	NP_005230.1:n.*992_*993del
NM_001256295.2:c.*992_*993del	NP_001243224.1:n.*992_*993del