Canonical Allele Identifier: CA2016614772

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11809639T= , CM000674.2:g.11809639T=	GRCh38
NC_000012.11:g.11962573T= , CM000674.1:g.11962573T=	GRCh37
NC_000012.10:g.11853840T=	NCBI36
NG_011443.1:g.164786T= , LRG_609:g.164786T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001987.5:c.164-29501T= MANE Select	NP_001978.1:n.164-29501T=
ENST00000396373.9:c.164-29501T= MANE Select	ENSP00000379658.3:n.164-29501T=
NM_001987.4:c.164-29501T= , LRG_609t1:c.164-29501T=	NP_001978.1:n.164-29501T=
ENST00000396373.8:c.164-29501T=	ENSP00000379658.3:n.164-29501T=
ENST00000541426.1:n.348-16005T=
ENST00000545027.1:c.80-29501T=	ENSP00000441463.1:n.80-29501T=
XM_011520607.1:c.161-29501T=	XP_011518909.1:n.161-29501T=
XM_011520607.2:c.161-29501T=	XP_011518909.1:n.161-29501T=
XM_011520608.1:c.137-29501T=	XP_011518910.1:n.137-29501T=
XM_011520608.2:c.137-29501T=	XP_011518910.1:n.137-29501T=
XM_011520611.1:c.-101-29501T=	XP_011518913.1:n.-101-29501T=
XM_011520611.2:c.-101-29501T=	XP_011518913.1:n.-101-29501T=
XM_017018990.1:c.164-29501T=	XP_016874479.1:n.164-29501T=
XM_017018991.1:c.-1497-16005T=	XP_016874480.1:n.-1497-16005T=