Canonical Allele Identifier: CA2016648614

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886029A= , CM000674.2:g.11886029A=	GRCh38
NC_000012.11:g.12038963A= , CM000674.1:g.12038963A=	GRCh37
NC_000012.10:g.11930230A=	NCBI36
NG_011443.1:g.241176A= , LRG_609:g.241176A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1253+3A= MANE Select	ENSP00000379658.3:n.1253+3A=
ENST00000266427.3:c.90+3A=
ENST00000396373.8:c.1253+3A=	ENSP00000379658.3:n.1253+3A=
NM_001987.4:c.1253+3A= , LRG_609t1:c.1253+3A=	NP_001978.1:n.1253+3A=
XM_011520607.1:c.1250+3A=	XP_011518909.1:n.1250+3A=
XM_011520608.1:c.1226+3A=	XP_011518910.1:n.1226+3A=
XM_011520609.1:c.989+3A=	XP_011518911.1:n.989+3A=
XM_011520610.1:c.989+3A=	XP_011518912.1:n.989+3A=
XM_011520611.1:c.989+3A=	XP_011518913.1:n.989+3A=
XM_011520612.1:c.632+3A=	XP_011518914.1:n.632+3A=
XM_011520607.2:c.1250+3A=	XP_011518909.1:n.1250+3A=
XM_011520608.2:c.1226+3A=	XP_011518910.1:n.1226+3A=
XM_011520609.2:c.989+3A=	XP_011518911.1:n.989+3A=
XM_011520611.2:c.989+3A=	XP_011518913.1:n.989+3A=
XM_011520612.2:c.632+3A=	XP_011518914.1:n.632+3A=
XM_017018990.1:c.1118+3A=	XP_016874479.1:n.1118+3A=
XM_017018991.1:c.989+3A=	XP_016874480.1:n.989+3A=
NM_001987.5:c.1253+3A= MANE Select	NP_001978.1:n.1253+3A=