Canonical Allele Identifier: CA232546168

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11752191dup , CM000674.2:g.11752191dup	GRCh38
NC_000012.11:g.11905125dup , CM000674.1:g.11905125dup	GRCh37
NC_000012.10:g.11796392dup	NCBI36
NG_011443.1:g.107338dup , LRG_609:g.107338dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.34-259dup MANE Select	ENSP00000379658.3:n.34-259dup
ENST00000396373.8:c.34-259dup	ENSP00000379658.3:n.34-259dup
ENST00000541426.1:n.218-259dup
ENST00000544715.1:n.308-259dup
NM_001987.4:c.34-259dup , LRG_609t1:c.34-259dup	NP_001978.1:n.34-259dup
XM_011520607.1:c.34-262dup	XP_011518909.1:n.34-262dup
XM_011520608.1:c.7-259dup	XP_011518910.1:n.7-259dup
XM_011520611.1:c.-101-86949dup	XP_011518913.1:n.-101-86949dup
XM_011520607.2:c.34-262dup	XP_011518909.1:n.34-262dup
XM_011520608.2:c.7-259dup	XP_011518910.1:n.7-259dup
XM_011520611.2:c.-101-86949dup	XP_011518913.1:n.-101-86949dup
XM_017018990.1:c.34-259dup	XP_016874479.1:n.34-259dup
XM_017018991.1:c.-1627-259dup	XP_016874480.1:n.-1627-259dup
NM_001987.5:c.34-259dup MANE Select	NP_001978.1:n.34-259dup