Canonical Allele Identifier: CA2016648479

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885728A= , CM000674.2:g.11885728A=	GRCh38
NC_000012.11:g.12038662A= , CM000674.1:g.12038662A=	GRCh37
NC_000012.10:g.11929929A=	NCBI36
NG_011443.1:g.240875A= , LRG_609:g.240875A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-198A= MANE Select	ENSP00000379658.3:n.1153-198A=
ENST00000396373.8:c.1153-198A=	ENSP00000379658.3:n.1153-198A=
NM_001987.4:c.1153-198A= , LRG_609t1:c.1153-198A=	NP_001978.1:n.1153-198A=
XM_011520607.1:c.1150-198A=	XP_011518909.1:n.1150-198A=
XM_011520608.1:c.1126-198A=	XP_011518910.1:n.1126-198A=
XM_011520609.1:c.889-198A=	XP_011518911.1:n.889-198A=
XM_011520610.1:c.889-198A=	XP_011518912.1:n.889-198A=
XM_011520611.1:c.889-198A=	XP_011518913.1:n.889-198A=
XM_011520612.1:c.532-198A=	XP_011518914.1:n.532-198A=
XM_011520607.2:c.1150-198A=	XP_011518909.1:n.1150-198A=
XM_011520608.2:c.1126-198A=	XP_011518910.1:n.1126-198A=
XM_011520609.2:c.889-198A=	XP_011518911.1:n.889-198A=
XM_011520611.2:c.889-198A=	XP_011518913.1:n.889-198A=
XM_011520612.2:c.532-198A=	XP_011518914.1:n.532-198A=
XM_017018990.1:c.1018-198A=	XP_016874479.1:n.1018-198A=
XM_017018991.1:c.889-198A=	XP_016874480.1:n.889-198A=
NM_001987.5:c.1153-198A= MANE Select	NP_001978.1:n.1153-198A=