Canonical Allele Identifier: CA2573053612

Gene: ETV6

Linked Data

• ClinVar Variation Id: 1338390
• ClinVar RCV Id: RCV001817761
• dbSNP Id: rs2136602130

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.11885924_11885938del , CM000674.2:g.11885924_11885938del	GRCh38
NC_000012.11:g.12038858_12038872del , CM000674.1:g.12038858_12038872del	GRCh37
NC_000012.10:g.11930125_11930139del	NCBI36
NG_011443.1:g.241071_241085del , LRG_609:g.241071_241085del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396373.9:c.1153-2_1165del
ENST00000396373.8:c.1153-2_1165del
NM_001987.4:c.1153-2_1165del , LRG_609t1:c.1153-2_1165del
XM_011520607.1:c.1150-2_1162del
XM_011520608.1:c.1126-2_1138del
XM_011520609.1:c.889-2_901del
XM_011520610.1:c.889-2_901del
XM_011520611.1:c.889-2_901del
XM_011520612.1:c.532-2_544del
XM_011520607.2:c.1150-2_1162del
XM_011520608.2:c.1126-2_1138del
XM_011520609.2:c.889-2_901del
XM_011520611.2:c.889-2_901del
XM_011520612.2:c.532-2_544del
XM_017018990.1:c.1018-2_1030del
XM_017018991.1:c.889-2_901del
NM_001987.5:c.1153-2_1165del