Canonical Allele Identifier: CA2617675032

Gene: ETV6

Linked Data

• gnomAD v4: 12-11885834-TTTTATTTTAATAGCTCCCGCAGTGCCTTTTCTGAGGTTCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885838_11885877del , CM000674.2:g.11885838_11885877del	GRCh38
NC_000012.11:g.12038772_12038811del , CM000674.1:g.12038772_12038811del	GRCh37
NC_000012.10:g.11930039_11930078del	NCBI36
NG_011443.1:g.240985_241024del , LRG_609:g.240985_241024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-88_1153-49del MANE Select	ENSP00000379658.3:n.1153-88_1153-49del
ENST00000396373.8:c.1153-88_1153-49del	ENSP00000379658.3:n.1153-88_1153-49del
NM_001987.4:c.1153-88_1153-49del , LRG_609t1:c.1153-88_1153-49del	NP_001978.1:n.1153-88_1153-49del
XM_011520607.1:c.1150-88_1150-49del	XP_011518909.1:n.1150-88_1150-49del
XM_011520608.1:c.1126-88_1126-49del	XP_011518910.1:n.1126-88_1126-49del
XM_011520609.1:c.889-88_889-49del	XP_011518911.1:n.889-88_889-49del
XM_011520610.1:c.889-88_889-49del	XP_011518912.1:n.889-88_889-49del
XM_011520611.1:c.889-88_889-49del	XP_011518913.1:n.889-88_889-49del
XM_011520612.1:c.532-88_532-49del	XP_011518914.1:n.532-88_532-49del
XM_011520607.2:c.1150-88_1150-49del	XP_011518909.1:n.1150-88_1150-49del
XM_011520608.2:c.1126-88_1126-49del	XP_011518910.1:n.1126-88_1126-49del
XM_011520609.2:c.889-88_889-49del	XP_011518911.1:n.889-88_889-49del
XM_011520611.2:c.889-88_889-49del	XP_011518913.1:n.889-88_889-49del
XM_011520612.2:c.532-88_532-49del	XP_011518914.1:n.532-88_532-49del
XM_017018990.1:c.1018-88_1018-49del	XP_016874479.1:n.1018-88_1018-49del
XM_017018991.1:c.889-88_889-49del	XP_016874480.1:n.889-88_889-49del
NM_001987.5:c.1153-88_1153-49del MANE Select	NP_001978.1:n.1153-88_1153-49del