Canonical Allele Identifier: CA2326387168

Gene: ELL

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.18508075_18508077delinsGCA , CM000681.2:g.18508075_18508077delinsGCA	GRCh38
NC_000019.9:g.18618885_18618887delinsGCA , CM000681.1:g.18618885_18618887delinsGCA	GRCh37
NC_000019.8:g.18479885_18479887delinsGCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262809.9:c.135+13844_135+13846delinsTGC MANE Select	ENSP00000262809.3:n.135+13844_135+13846delinsTGC
ENST00000262809.8:c.135+13844_135+13846delinsTGC	ENSP00000262809.3:n.135+13844_135+13846delinsTGC
ENST00000594635.6:c.135+13844_135+13846delinsTGC	ENSP00000475681.2:n.135+13844_135+13846delinsTGC
ENST00000596915.1:n.147+13844_147+13846delinsTGC
NM_006532.3:c.135+13844_135+13846delinsTGC	NP_006523.1:n.135+13844_135+13846delinsTGC
XM_011528330.1:c.135+13844_135+13846delinsTGC	XP_011526632.1:n.135+13844_135+13846delinsTGC
XR_936207.1:n.209+13844_209+13846delinsTGC
XM_011528330.3:c.135+13844_135+13846delinsTGC	XP_011526632.2:n.135+13844_135+13846delinsTGC
XM_017027335.1:c.-385+13844_-385+13846delinsTGC	XP_016882824.1:n.-385+13844_-385+13846delinsTGC
XR_001753769.2:n.140+13844_140+13846delinsTGC
XR_936207.3:n.140+13844_140+13846delinsTGC
NM_006532.4:c.135+13844_135+13846delinsTGC MANE Select	NP_006523.1:n.135+13844_135+13846delinsTGC