Canonical Allele Identifier: CA2617674999
Gene: ETV6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.11885811_11885824del , CM000674.2:g.11885811_11885824del GRCh38
NC_000012.11:g.12038745_12038758del , CM000674.1:g.12038745_12038758del GRCh37
NC_000012.10:g.11930012_11930025del NCBI36
NG_011443.1:g.240958_240971del , LRG_609:g.240958_240971del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396373.9:c.1153-115_1153-102del MANE Select ENSP00000379658.3:n.1153-115_1153-102del
ENST00000396373.8:c.1153-115_1153-102del ENSP00000379658.3:n.1153-115_1153-102del
NM_001987.4:c.1153-115_1153-102del , LRG_609t1:c.1153-115_1153-102del NP_001978.1:n.1153-115_1153-102del
XM_011520607.1:c.1150-115_1150-102del XP_011518909.1:n.1150-115_1150-102del
XM_011520608.1:c.1126-115_1126-102del XP_011518910.1:n.1126-115_1126-102del
XM_011520609.1:c.889-115_889-102del XP_011518911.1:n.889-115_889-102del
XM_011520610.1:c.889-115_889-102del XP_011518912.1:n.889-115_889-102del
XM_011520611.1:c.889-115_889-102del XP_011518913.1:n.889-115_889-102del
XM_011520612.1:c.532-115_532-102del XP_011518914.1:n.532-115_532-102del
XM_011520607.2:c.1150-115_1150-102del XP_011518909.1:n.1150-115_1150-102del
XM_011520608.2:c.1126-115_1126-102del XP_011518910.1:n.1126-115_1126-102del
XM_011520609.2:c.889-115_889-102del XP_011518911.1:n.889-115_889-102del
XM_011520611.2:c.889-115_889-102del XP_011518913.1:n.889-115_889-102del
XM_011520612.2:c.532-115_532-102del XP_011518914.1:n.532-115_532-102del
XM_017018990.1:c.1018-115_1018-102del XP_016874479.1:n.1018-115_1018-102del
XM_017018991.1:c.889-115_889-102del XP_016874480.1:n.889-115_889-102del
NM_001987.5:c.1153-115_1153-102del MANE Select NP_001978.1:n.1153-115_1153-102del