Canonical Allele Identifier: CA2016648470

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885712G= , CM000674.2:g.11885712G=	GRCh38
NC_000012.11:g.12038646G= , CM000674.1:g.12038646G=	GRCh37
NC_000012.10:g.11929913G=	NCBI36
NG_011443.1:g.240859G= , LRG_609:g.240859G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-214G= MANE Select	ENSP00000379658.3:n.1153-214G=
ENST00000396373.8:c.1153-214G=	ENSP00000379658.3:n.1153-214G=
NM_001987.4:c.1153-214G= , LRG_609t1:c.1153-214G=	NP_001978.1:n.1153-214G=
XM_011520607.1:c.1150-214G=	XP_011518909.1:n.1150-214G=
XM_011520608.1:c.1126-214G=	XP_011518910.1:n.1126-214G=
XM_011520609.1:c.889-214G=	XP_011518911.1:n.889-214G=
XM_011520610.1:c.889-214G=	XP_011518912.1:n.889-214G=
XM_011520611.1:c.889-214G=	XP_011518913.1:n.889-214G=
XM_011520612.1:c.532-214G=	XP_011518914.1:n.532-214G=
XM_011520607.2:c.1150-214G=	XP_011518909.1:n.1150-214G=
XM_011520608.2:c.1126-214G=	XP_011518910.1:n.1126-214G=
XM_011520609.2:c.889-214G=	XP_011518911.1:n.889-214G=
XM_011520611.2:c.889-214G=	XP_011518913.1:n.889-214G=
XM_011520612.2:c.532-214G=	XP_011518914.1:n.532-214G=
XM_017018990.1:c.1018-214G=	XP_016874479.1:n.1018-214G=
XM_017018991.1:c.889-214G=	XP_016874480.1:n.889-214G=
NM_001987.5:c.1153-214G= MANE Select	NP_001978.1:n.1153-214G=