Canonical Allele Identifier: CA2016648599

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885974T= , CM000674.2:g.11885974T=	GRCh38
NC_000012.11:g.12038908T= , CM000674.1:g.12038908T=	GRCh37
NC_000012.10:g.11930175T=	NCBI36
NG_011443.1:g.241121T= , LRG_609:g.241121T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1201T= MANE Select	ENSP00000379658.3:p.Tyr401=
ENST00000266427.3:c.38T=
ENST00000396373.8:c.1201T=	ENSP00000379658.3:p.Tyr401=
NM_001987.4:c.1201T= , LRG_609t1:c.1201T=	NP_001978.1:p.Tyr401=
XM_011520607.1:c.1198T=	XP_011518909.1:p.Tyr400=
XM_011520608.1:c.1174T=	XP_011518910.1:p.Tyr392=
XM_011520609.1:c.937T=	XP_011518911.1:p.Tyr313=
XM_011520610.1:c.937T=	XP_011518912.1:p.Tyr313=
XM_011520611.1:c.937T=	XP_011518913.1:p.Tyr313=
XM_011520612.1:c.580T=	XP_011518914.1:p.Tyr194=
XM_011520607.2:c.1198T=	XP_011518909.1:p.Tyr400=
XM_011520608.2:c.1174T=	XP_011518910.1:p.Tyr392=
XM_011520609.2:c.937T=	XP_011518911.1:p.Tyr313=
XM_011520611.2:c.937T=	XP_011518913.1:p.Tyr313=
XM_011520612.2:c.580T=	XP_011518914.1:p.Tyr194=
XM_017018990.1:c.1066T=	XP_016874479.1:p.Tyr356=
XM_017018991.1:c.937T=	XP_016874480.1:p.Tyr313=
NM_001987.5:c.1201T= MANE Select	NP_001978.1:p.Tyr401=