Canonical Allele Identifier: CA2725554085
Gene: ETV6 HGNC NCBI

Linked Data

dbSNP Id: rs2136602329

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11885969_11885970insGGAG , CM000674.2:g.11885969_11885970insGGAG GRCh38
NC_000012.11:g.12038903_12038904insGGAG , CM000674.1:g.12038903_12038904insGGAG GRCh37
NC_000012.10:g.11930170_11930171insGGAG NCBI36
NG_011443.1:g.241116_241117insGGAG , LRG_609:g.241116_241117insGGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.1196_1197insGGAG MANE Select ENSP00000379658.3:p.His400GlufsTer27
ENST00000266427.3:c.33_34insGGAG
ENST00000396373.8:c.1196_1197insGGAG ENSP00000379658.3:p.His400GlufsTer27
NM_001987.4:c.1196_1197insGGAG , LRG_609t1:c.1196_1197insGGAG NP_001978.1:p.His400GlufsTer27
XM_011520607.1:c.1193_1194insGGAG XP_011518909.1:p.His399GlufsTer27
XM_011520608.1:c.1169_1170insGGAG XP_011518910.1:p.His391GlufsTer27
XM_011520609.1:c.932_933insGGAG XP_011518911.1:p.His312GlufsTer27
XM_011520610.1:c.932_933insGGAG XP_011518912.1:p.His312GlufsTer27
XM_011520611.1:c.932_933insGGAG XP_011518913.1:p.His312GlufsTer27
XM_011520612.1:c.575_576insGGAG XP_011518914.1:p.His193GlufsTer27
XM_011520607.2:c.1193_1194insGGAG XP_011518909.1:p.His399GlufsTer27
XM_011520608.2:c.1169_1170insGGAG XP_011518910.1:p.His391GlufsTer27
XM_011520609.2:c.932_933insGGAG XP_011518911.1:p.His312GlufsTer27
XM_011520611.2:c.932_933insGGAG XP_011518913.1:p.His312GlufsTer27
XM_011520612.2:c.575_576insGGAG XP_011518914.1:p.His193GlufsTer27
XM_017018990.1:c.1061_1062insGGAG XP_016874479.1:p.His355GlufsTer27
XM_017018991.1:c.932_933insGGAG XP_016874480.1:p.His312GlufsTer27
NM_001987.5:c.1196_1197insGGAG MANE Select NP_001978.1:p.His400GlufsTer27