Canonical Allele Identifier: CA2016648583

Gene: ETV6

Linked Data

• dbSNP Id: rs1947176451

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885911_11885913dup , CM000674.2:g.11885911_11885913dup	GRCh38
NC_000012.11:g.12038845_12038847dup , CM000674.1:g.12038845_12038847dup	GRCh37
NC_000012.10:g.11930112_11930114dup	NCBI36
NG_011443.1:g.241058_241060dup , LRG_609:g.241058_241060dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-15_1153-13dup MANE Select	ENSP00000379658.3:n.1153-15_1153-13dup
ENST00000396373.8:c.1153-15_1153-13dup	ENSP00000379658.3:n.1153-15_1153-13dup
NM_001987.4:c.1153-15_1153-13dup , LRG_609t1:c.1153-15_1153-13dup	NP_001978.1:n.1153-15_1153-13dup
XM_011520607.1:c.1150-15_1150-13dup	XP_011518909.1:n.1150-15_1150-13dup
XM_011520608.1:c.1126-15_1126-13dup	XP_011518910.1:n.1126-15_1126-13dup
XM_011520609.1:c.889-15_889-13dup	XP_011518911.1:n.889-15_889-13dup
XM_011520610.1:c.889-15_889-13dup	XP_011518912.1:n.889-15_889-13dup
XM_011520611.1:c.889-15_889-13dup	XP_011518913.1:n.889-15_889-13dup
XM_011520612.1:c.532-15_532-13dup	XP_011518914.1:n.532-15_532-13dup
XM_011520607.2:c.1150-15_1150-13dup	XP_011518909.1:n.1150-15_1150-13dup
XM_011520608.2:c.1126-15_1126-13dup	XP_011518910.1:n.1126-15_1126-13dup
XM_011520609.2:c.889-15_889-13dup	XP_011518911.1:n.889-15_889-13dup
XM_011520611.2:c.889-15_889-13dup	XP_011518913.1:n.889-15_889-13dup
XM_011520612.2:c.532-15_532-13dup	XP_011518914.1:n.532-15_532-13dup
XM_017018990.1:c.1018-15_1018-13dup	XP_016874479.1:n.1018-15_1018-13dup
XM_017018991.1:c.889-15_889-13dup	XP_016874480.1:n.889-15_889-13dup
NM_001987.5:c.1153-15_1153-13dup MANE Select	NP_001978.1:n.1153-15_1153-13dup