Canonical Allele Identifier: CA2016585120

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11747039G= , CM000674.2:g.11747039G=	GRCh38
NC_000012.11:g.11899973G= , CM000674.1:g.11899973G=	GRCh37
NC_000012.10:g.11791240G=	NCBI36
NG_011443.1:g.102186G= , LRG_609:g.102186G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001987.5:c.34-5411G= MANE Select	NP_001978.1:n.34-5411G=
ENST00000396373.9:c.34-5411G= MANE Select	ENSP00000379658.3:n.34-5411G=
NM_001987.4:c.34-5411G= , LRG_609t1:c.34-5411G=	NP_001978.1:n.34-5411G=
ENST00000396373.8:c.34-5411G=	ENSP00000379658.3:n.34-5411G=
ENST00000541426.1:n.218-5411G=
ENST00000544715.1:n.308-5411G=
XM_011520607.1:c.34-5414G=	XP_011518909.1:n.34-5414G=
XM_011520607.2:c.34-5414G=	XP_011518909.1:n.34-5414G=
XM_011520608.1:c.6+3097G=	XP_011518910.1:n.6+3097G=
XM_011520608.2:c.6+3097G=	XP_011518910.1:n.6+3097G=
XM_011520611.1:c.-101-92101G=	XP_011518913.1:n.-101-92101G=
XM_011520611.2:c.-101-92101G=	XP_011518913.1:n.-101-92101G=
XM_017018990.1:c.34-5411G=	XP_016874479.1:n.34-5411G=
XM_017018991.1:c.-1627-5411G=	XP_016874480.1:n.-1627-5411G=