Canonical Allele Identifier: CA2794567708

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885837_11885858del , CM000674.2:g.11885837_11885858del	GRCh38
NC_000012.11:g.12038771_12038792del , CM000674.1:g.12038771_12038792del	GRCh37
NC_000012.10:g.11930038_11930059del	NCBI36
NG_011443.1:g.240984_241005del , LRG_609:g.240984_241005del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-89_1153-68del MANE Select	ENSP00000379658.3:n.1153-89_1153-68del
ENST00000396373.8:c.1153-89_1153-68del	ENSP00000379658.3:n.1153-89_1153-68del
NM_001987.4:c.1153-89_1153-68del , LRG_609t1:c.1153-89_1153-68del	NP_001978.1:n.1153-89_1153-68del
XM_011520607.1:c.1150-89_1150-68del	XP_011518909.1:n.1150-89_1150-68del
XM_011520608.1:c.1126-89_1126-68del	XP_011518910.1:n.1126-89_1126-68del
XM_011520609.1:c.889-89_889-68del	XP_011518911.1:n.889-89_889-68del
XM_011520610.1:c.889-89_889-68del	XP_011518912.1:n.889-89_889-68del
XM_011520611.1:c.889-89_889-68del	XP_011518913.1:n.889-89_889-68del
XM_011520612.1:c.532-89_532-68del	XP_011518914.1:n.532-89_532-68del
XM_011520607.2:c.1150-89_1150-68del	XP_011518909.1:n.1150-89_1150-68del
XM_011520608.2:c.1126-89_1126-68del	XP_011518910.1:n.1126-89_1126-68del
XM_011520609.2:c.889-89_889-68del	XP_011518911.1:n.889-89_889-68del
XM_011520611.2:c.889-89_889-68del	XP_011518913.1:n.889-89_889-68del
XM_011520612.2:c.532-89_532-68del	XP_011518914.1:n.532-89_532-68del
XM_017018990.1:c.1018-89_1018-68del	XP_016874479.1:n.1018-89_1018-68del
XM_017018991.1:c.889-89_889-68del	XP_016874480.1:n.889-89_889-68del
NM_001987.5:c.1153-89_1153-68del MANE Select	NP_001978.1:n.1153-89_1153-68del