Canonical Allele Identifier: CA281475
Gene: ELN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.74056273del , CM000669.2:g.74056273del GRCh38
NC_000007.13:g.73470603del , CM000669.1:g.73470603del GRCh37
NC_000007.12:g.73108539del NCBI36
NG_009261.1:g.33177del

Transcript Alleles

HGVS Amino-acid Change
ENST00000692049.1:c.1153del
ENST00000252034.12:c.1153del
ENST00000252034.11:c.1153del
ENST00000320399.10:c.1153del
ENST00000320492.11:c.1045del
ENST00000357036.9:c.1168del
ENST00000358929.8:c.1153del
ENST00000380553.8:c.802del
ENST00000380562.8:c.1153del
ENST00000380575.8:c.1123del
ENST00000380576.9:c.1153del
ENST00000380584.8:c.1111del
ENST00000414324.5:c.1138del
ENST00000429192.5:c.1168del
ENST00000445912.5:c.1153del
ENST00000458204.5:c.1123del
ENST00000466878.5:n.472del
ENST00000492210.1:n.516del
ENST00000621115.4:c.1021del
NM_000501.3:c.1153del
NM_001081752.2:c.1123del
NM_001081753.2:c.1168del
NM_001081754.2:c.1168del
NM_001081755.2:c.1153del
NM_001278912.1:c.1153del
NM_001278913.1:c.1045del
NM_001278914.1:c.1138del
NM_001278915.1:c.1153del
NM_001278916.1:c.1111del
NM_001278917.1:c.1123del
NM_001278918.1:c.1021del
NM_001278939.1:c.1153del
XM_005250187.1:c.1117del
XM_005250188.1:c.1111del
XM_011515868.1:c.1168del
XM_011515869.1:c.1138del
XM_011515870.1:c.1132del
XM_011515871.1:c.1126del
XM_011515872.1:c.1114del
XM_011515873.1:c.1168del
XM_011515874.1:c.1102del
XM_011515875.1:c.1087del
XM_011515876.1:c.1168del
XM_011515877.1:c.1114del
XM_005250187.2:c.1117del
XM_005250188.2:c.1111del
XM_011515868.2:c.1168del
XM_011515871.2:c.1126del
XM_011515872.2:c.1114del
XM_011515873.2:c.1168del
XM_011515875.2:c.1087del
XM_011515876.2:c.1168del
XM_011515877.2:c.1114del
XM_017011813.1:c.1081del
XM_017011814.2:c.1126del
NM_000501.4:c.1153del
NM_001081752.3:c.1123del
NM_001081753.3:c.1168del
NM_001081754.3:c.1168del
NM_001081755.3:c.1153del
NM_001278912.2:c.1153del
NM_001278913.2:c.1045del
NM_001278914.2:c.1138del
NM_001278915.2:c.1153del
NM_001278916.2:c.1111del
NM_001278917.2:c.1123del
NM_001278918.2:c.1021del
NM_001278939.2:c.1153del