Canonical Allele Identifier: CA478767188

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11884578A>T , CM000674.2:g.11884578A>T	GRCh38
NC_000012.11:g.12037512A>T , CM000674.1:g.12037512A>T	GRCh37
NC_000012.10:g.11928779A>T	NCBI36
NG_011443.1:g.239725A>T , LRG_609:g.239725A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1143A>T MANE Select	ENSP00000379658.3:p.Gly381=
ENST00000396373.8:c.1143A>T	ENSP00000379658.3:p.Gly381=
NM_001987.4:c.1143A>T , LRG_609t1:c.1143A>T	NP_001978.1:p.Gly381=
XM_011520607.1:c.1140A>T	XP_011518909.1:p.Gly380=
XM_011520608.1:c.1116A>T	XP_011518910.1:p.Gly372=
XM_011520609.1:c.879A>T	XP_011518911.1:p.Gly293=
XM_011520610.1:c.879A>T	XP_011518912.1:p.Gly293=
XM_011520611.1:c.879A>T	XP_011518913.1:p.Gly293=
XM_011520612.1:c.522A>T	XP_011518914.1:p.Gly174=
XM_011520607.2:c.1140A>T	XP_011518909.1:p.Gly380=
XM_011520608.2:c.1116A>T	XP_011518910.1:p.Gly372=
XM_011520609.2:c.879A>T	XP_011518911.1:p.Gly293=
XM_011520611.2:c.879A>T	XP_011518913.1:p.Gly293=
XM_011520612.2:c.522A>T	XP_011518914.1:p.Gly174=
XM_017018990.1:c.1008A>T	XP_016874479.1:p.Gly336=
XM_017018991.1:c.879A>T	XP_016874480.1:p.Gly293=
NM_001987.5:c.1143A>T MANE Select	NP_001978.1:p.Gly381=