Canonical Allele Identifier: CA2016648530
Gene: ETV6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11885816_11885817delinsAG , CM000674.2:g.11885816_11885817delinsAG GRCh38
NC_000012.11:g.12038750_12038751delinsAG , CM000674.1:g.12038750_12038751delinsAG GRCh37
NC_000012.10:g.11930017_11930018delinsAG NCBI36
NG_011443.1:g.240963_240964delinsAG , LRG_609:g.240963_240964delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.1153-110_1153-109delinsAG MANE Select ENSP00000379658.3:n.1153-110_1153-109delinsAG
ENST00000396373.8:c.1153-110_1153-109delinsAG ENSP00000379658.3:n.1153-110_1153-109delinsAG
NM_001987.4:c.1153-110_1153-109delinsAG , LRG_609t1:c.1153-110_1153-109delinsAG NP_001978.1:n.1153-110_1153-109delinsAG
XM_011520607.1:c.1150-110_1150-109delinsAG XP_011518909.1:n.1150-110_1150-109delinsAG
XM_011520608.1:c.1126-110_1126-109delinsAG XP_011518910.1:n.1126-110_1126-109delinsAG
XM_011520609.1:c.889-110_889-109delinsAG XP_011518911.1:n.889-110_889-109delinsAG
XM_011520610.1:c.889-110_889-109delinsAG XP_011518912.1:n.889-110_889-109delinsAG
XM_011520611.1:c.889-110_889-109delinsAG XP_011518913.1:n.889-110_889-109delinsAG
XM_011520612.1:c.532-110_532-109delinsAG XP_011518914.1:n.532-110_532-109delinsAG
XM_011520607.2:c.1150-110_1150-109delinsAG XP_011518909.1:n.1150-110_1150-109delinsAG
XM_011520608.2:c.1126-110_1126-109delinsAG XP_011518910.1:n.1126-110_1126-109delinsAG
XM_011520609.2:c.889-110_889-109delinsAG XP_011518911.1:n.889-110_889-109delinsAG
XM_011520611.2:c.889-110_889-109delinsAG XP_011518913.1:n.889-110_889-109delinsAG
XM_011520612.2:c.532-110_532-109delinsAG XP_011518914.1:n.532-110_532-109delinsAG
XM_017018990.1:c.1018-110_1018-109delinsAG XP_016874479.1:n.1018-110_1018-109delinsAG
XM_017018991.1:c.889-110_889-109delinsAG XP_016874480.1:n.889-110_889-109delinsAG
NM_001987.5:c.1153-110_1153-109delinsAG MANE Select NP_001978.1:n.1153-110_1153-109delinsAG