Canonical Allele Identifier: CA2580085156
Gene: ETV6 HGNC NCBI

Linked Data

ClinVar Variation Id: 2035436
ClinVar RCV Id: RCV002890031

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11885925_11885926del , CM000674.2:g.11885925_11885926del GRCh38
NC_000012.11:g.12038859_12038860del , CM000674.1:g.12038859_12038860del GRCh37
NC_000012.10:g.11930126_11930127del NCBI36
NG_011443.1:g.241072_241073del , LRG_609:g.241072_241073del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.1153-1_1153del
ENST00000396373.8:c.1153-1_1153del
NM_001987.4:c.1153-1_1153del , LRG_609t1:c.1153-1_1153del
XM_011520607.1:c.1150-1_1150del
XM_011520608.1:c.1126-1_1126del
XM_011520609.1:c.889-1_889del
XM_011520610.1:c.889-1_889del
XM_011520611.1:c.889-1_889del
XM_011520612.1:c.532-1_532del
XM_011520607.2:c.1150-1_1150del
XM_011520608.2:c.1126-1_1126del
XM_011520609.2:c.889-1_889del
XM_011520611.2:c.889-1_889del
XM_011520612.2:c.532-1_532del
XM_017018990.1:c.1018-1_1018del
XM_017018991.1:c.889-1_889del
NM_001987.5:c.1153-1_1153del