Canonical Allele Identifier: CA2580609246

Gene: ETS2

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.38822185G>A , CM000683.2:g.38822185G>A	GRCh38
NC_000021.8:g.40194109G>A , CM000683.1:g.40194109G>A	GRCh37
NC_000021.7:g.39115979G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360214.8:c.1194+481G>A	ENSP00000353344.3:n.1194+481G>A
ENST00000360938.8:c.1194+481G>A MANE Select	ENSP00000354194.3:n.1194+481G>A
ENST00000653642.1:c.1194+481G>A	ENSP00000499315.1:n.1194+481G>A
ENST00000662305.1:c.1194+481G>A	ENSP00000499226.1:n.1194+481G>A
ENST00000666778.1:c.1194+481G>A	ENSP00000499775.1:n.1194+481G>A
ENST00000667466.1:c.1299+481G>A	ENSP00000499540.1:n.1299+481G>A
ENST00000360214.7:c.1194+481G>A	ENSP00000353344.3:n.1194+481G>A
ENST00000360938.7:c.1194+481G>A	ENSP00000354194.3:n.1194+481G>A
NM_001256295.1:c.1614+481G>A	NP_001243224.1:n.1614+481G>A
NM_005239.5:c.1194+481G>A	NP_005230.1:n.1194+481G>A
XM_005260935.1:c.1194+481G>A	XP_005260992.1:n.1194+481G>A
XM_017028290.1:c.1194+481G>A	XP_016883779.1:n.1194+481G>A
NM_005239.6:c.1194+481G>A MANE Select	NP_005230.1:n.1194+481G>A
NM_001256295.2:c.1614+481G>A	NP_001243224.1:n.1614+481G>A