Canonical Allele Identifier: CA2725554087

Gene: ETV6

Linked Data

• dbSNP Id: rs2136602475

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11886005del , CM000674.2:g.11886005del	GRCh38
NC_000012.11:g.12038939del , CM000674.1:g.12038939del	GRCh37
NC_000012.10:g.11930206del	NCBI36
NG_011443.1:g.241152del , LRG_609:g.241152del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1232del MANE Select	ENSP00000379658.3:p.Pro411GlnfsTer10
ENST00000266427.3:c.69del
ENST00000396373.8:c.1232del	ENSP00000379658.3:p.Pro411GlnfsTer10
NM_001987.4:c.1232del , LRG_609t1:c.1232del	NP_001978.1:p.Pro411GlnfsTer10
XM_011520607.1:c.1229del	XP_011518909.1:p.Pro410GlnfsTer10
XM_011520608.1:c.1205del	XP_011518910.1:p.Pro402GlnfsTer10
XM_011520609.1:c.968del	XP_011518911.1:p.Pro323GlnfsTer10
XM_011520610.1:c.968del	XP_011518912.1:p.Pro323GlnfsTer10
XM_011520611.1:c.968del	XP_011518913.1:p.Pro323GlnfsTer10
XM_011520612.1:c.611del	XP_011518914.1:p.Pro204GlnfsTer10
XM_011520607.2:c.1229del	XP_011518909.1:p.Pro410GlnfsTer10
XM_011520608.2:c.1205del	XP_011518910.1:p.Pro402GlnfsTer10
XM_011520609.2:c.968del	XP_011518911.1:p.Pro323GlnfsTer10
XM_011520611.2:c.968del	XP_011518913.1:p.Pro323GlnfsTer10
XM_011520612.2:c.611del	XP_011518914.1:p.Pro204GlnfsTer10
XM_017018990.1:c.1097del	XP_016874479.1:p.Pro366GlnfsTer10
XM_017018991.1:c.968del	XP_016874480.1:p.Pro323GlnfsTer10
NM_001987.5:c.1232del MANE Select	NP_001978.1:p.Pro411GlnfsTer10