Canonical Allele Identifier: CA2016648486
Gene: ETV6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11885738_11885739delinsTA , CM000674.2:g.11885738_11885739delinsTA GRCh38
NC_000012.11:g.12038672_12038673delinsTA , CM000674.1:g.12038672_12038673delinsTA GRCh37
NC_000012.10:g.11929939_11929940delinsTA NCBI36
NG_011443.1:g.240885_240886delinsTA , LRG_609:g.240885_240886delinsTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.1153-188_1153-187delinsTA MANE Select ENSP00000379658.3:n.1153-188_1153-187delinsTA
ENST00000396373.8:c.1153-188_1153-187delinsTA ENSP00000379658.3:n.1153-188_1153-187delinsTA
NM_001987.4:c.1153-188_1153-187delinsTA , LRG_609t1:c.1153-188_1153-187delinsTA NP_001978.1:n.1153-188_1153-187delinsTA
XM_011520607.1:c.1150-188_1150-187delinsTA XP_011518909.1:n.1150-188_1150-187delinsTA
XM_011520608.1:c.1126-188_1126-187delinsTA XP_011518910.1:n.1126-188_1126-187delinsTA
XM_011520609.1:c.889-188_889-187delinsTA XP_011518911.1:n.889-188_889-187delinsTA
XM_011520610.1:c.889-188_889-187delinsTA XP_011518912.1:n.889-188_889-187delinsTA
XM_011520611.1:c.889-188_889-187delinsTA XP_011518913.1:n.889-188_889-187delinsTA
XM_011520612.1:c.532-188_532-187delinsTA XP_011518914.1:n.532-188_532-187delinsTA
XM_011520607.2:c.1150-188_1150-187delinsTA XP_011518909.1:n.1150-188_1150-187delinsTA
XM_011520608.2:c.1126-188_1126-187delinsTA XP_011518910.1:n.1126-188_1126-187delinsTA
XM_011520609.2:c.889-188_889-187delinsTA XP_011518911.1:n.889-188_889-187delinsTA
XM_011520611.2:c.889-188_889-187delinsTA XP_011518913.1:n.889-188_889-187delinsTA
XM_011520612.2:c.532-188_532-187delinsTA XP_011518914.1:n.532-188_532-187delinsTA
XM_017018990.1:c.1018-188_1018-187delinsTA XP_016874479.1:n.1018-188_1018-187delinsTA
XM_017018991.1:c.889-188_889-187delinsTA XP_016874480.1:n.889-188_889-187delinsTA
NM_001987.5:c.1153-188_1153-187delinsTA MANE Select NP_001978.1:n.1153-188_1153-187delinsTA