Canonical Allele Identifier: CA2016648519

Gene: ETV6

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885786_11885814delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA , CM000674.2:g.11885786_11885814delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	GRCh38
NC_000012.11:g.12038720_12038748delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA , CM000674.1:g.12038720_12038748delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	GRCh37
NC_000012.10:g.11929987_11930015delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	NCBI36
NG_011443.1:g.240933_240961delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA , LRG_609:g.240933_240961delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-140_1153-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA MANE Select	ENSP00000379658.3:n.1153-140_1153-112delinsGCAGGTAGCTTCCCAAAC...
ENST00000396373.8:c.1153-140_1153-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	ENSP00000379658.3:n.1153-140_1153-112delinsGCAGGTAGCTTCCCAAAC...
NM_001987.4:c.1153-140_1153-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA , LRG_609t1:c.1153-140_1153-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	NP_001978.1:n.1153-140_1153-112delinsGCAGGTAGCTTCCCAAACTGGCAG...
XM_011520607.1:c.1150-140_1150-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518909.1:n.1150-140_1150-112delinsGCAGGTAGCTTCCCAAACTGG...
XM_011520608.1:c.1126-140_1126-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518910.1:n.1126-140_1126-112delinsGCAGGTAGCTTCCCAAACTGG...
XM_011520609.1:c.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518911.1:n.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCA...
XM_011520610.1:c.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518912.1:n.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCA...
XM_011520611.1:c.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518913.1:n.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCA...
XM_011520612.1:c.532-140_532-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518914.1:n.532-140_532-112delinsGCAGGTAGCTTCCCAAACTGGCA...
XM_011520607.2:c.1150-140_1150-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518909.1:n.1150-140_1150-112delinsGCAGGTAGCTTCCCAAACTGG...
XM_011520608.2:c.1126-140_1126-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518910.1:n.1126-140_1126-112delinsGCAGGTAGCTTCCCAAACTGG...
XM_011520609.2:c.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518911.1:n.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCA...
XM_011520611.2:c.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518913.1:n.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCA...
XM_011520612.2:c.532-140_532-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_011518914.1:n.532-140_532-112delinsGCAGGTAGCTTCCCAAACTGGCA...
XM_017018990.1:c.1018-140_1018-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_016874479.1:n.1018-140_1018-112delinsGCAGGTAGCTTCCCAAACTGG...
XM_017018991.1:c.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA	XP_016874480.1:n.889-140_889-112delinsGCAGGTAGCTTCCCAAACTGGCA...
NM_001987.5:c.1153-140_1153-112delinsGCAGGTAGCTTCCCAAACTGGCAGGGCCA MANE Select	NP_001978.1:n.1153-140_1153-112delinsGCAGGTAGCTTCCCAAACTGGCAG...