Canonical Allele Identifier: CA2016614011

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11807938A= , CM000674.2:g.11807938A=	GRCh38
NC_000012.11:g.11960872A= , CM000674.1:g.11960872A=	GRCh37
NC_000012.10:g.11852139A=	NCBI36
NG_011443.1:g.163085A= , LRG_609:g.163085A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001987.5:c.164-31202A= MANE Select	NP_001978.1:n.164-31202A=
ENST00000396373.9:c.164-31202A= MANE Select	ENSP00000379658.3:n.164-31202A=
NM_001987.4:c.164-31202A= , LRG_609t1:c.164-31202A=	NP_001978.1:n.164-31202A=
ENST00000396373.8:c.164-31202A=	ENSP00000379658.3:n.164-31202A=
ENST00000541426.1:n.348-17706A=
ENST00000545027.1:c.80-31202A=	ENSP00000441463.1:n.80-31202A=
XM_011520607.1:c.161-31202A=	XP_011518909.1:n.161-31202A=
XM_011520607.2:c.161-31202A=	XP_011518909.1:n.161-31202A=
XM_011520608.1:c.137-31202A=	XP_011518910.1:n.137-31202A=
XM_011520608.2:c.137-31202A=	XP_011518910.1:n.137-31202A=
XM_011520611.1:c.-101-31202A=	XP_011518913.1:n.-101-31202A=
XM_011520611.2:c.-101-31202A=	XP_011518913.1:n.-101-31202A=
XM_017018990.1:c.164-31202A=	XP_016874479.1:n.164-31202A=
XM_017018991.1:c.-1497-17706A=	XP_016874480.1:n.-1497-17706A=