Canonical Allele Identifier: CA2016648612

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886025A= , CM000674.2:g.11886025A=	GRCh38
NC_000012.11:g.12038959A= , CM000674.1:g.12038959A=	GRCh37
NC_000012.10:g.11930226A=	NCBI36
NG_011443.1:g.241172A= , LRG_609:g.241172A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1252A= MANE Select	ENSP00000379658.3:p.Arg418=
ENST00000266427.3:c.89A=
ENST00000396373.8:c.1252A=	ENSP00000379658.3:p.Arg418=
NM_001987.4:c.1252A= , LRG_609t1:c.1252A=	NP_001978.1:p.Arg418=
XM_011520607.1:c.1249A=	XP_011518909.1:p.Arg417=
XM_011520608.1:c.1225A=	XP_011518910.1:p.Arg409=
XM_011520609.1:c.988A=	XP_011518911.1:p.Arg330=
XM_011520610.1:c.988A=	XP_011518912.1:p.Arg330=
XM_011520611.1:c.988A=	XP_011518913.1:p.Arg330=
XM_011520612.1:c.631A=	XP_011518914.1:p.Arg211=
XM_011520607.2:c.1249A=	XP_011518909.1:p.Arg417=
XM_011520608.2:c.1225A=	XP_011518910.1:p.Arg409=
XM_011520609.2:c.988A=	XP_011518911.1:p.Arg330=
XM_011520611.2:c.988A=	XP_011518913.1:p.Arg330=
XM_011520612.2:c.631A=	XP_011518914.1:p.Arg211=
XM_017018990.1:c.1117A=	XP_016874479.1:p.Arg373=
XM_017018991.1:c.988A=	XP_016874480.1:p.Arg330=
NM_001987.5:c.1252A= MANE Select	NP_001978.1:p.Arg418=