Canonical Allele Identifier: CA398222281
Gene: ELAC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.12992964C>A , CM000679.2:g.12992964C>A GRCh38
NC_000017.10:g.12896281C>A , CM000679.1:g.12896281C>A GRCh37
NC_000017.9:g.12837006C>A NCBI36
NG_015808.1:g.30101G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338034.9:c.2335G>T MANE Select ENSP00000337445.4:p.Glu779Ter
ENST00000338034.8:c.2335G>T ENSP00000337445.4:p.Glu779Ter
ENST00000395962.6:c.2278G>T ENSP00000379291.1:p.Glu760Ter
ENST00000426905.7:c.2215G>T ENSP00000405223.3:p.Glu739Ter
ENST00000465825.5:n.2222G>T
ENST00000480891.5:n.2164G>T
ENST00000484122.5:n.3165G>T
ENST00000487229.6:n.1881G>T
ENST00000584650.5:c.1734G>T
NM_001165962.1:c.2215G>T NP_001159434.1:p.Glu739Ter
NM_018127.6:c.2335G>T NP_060597.4:p.Glu779Ter
NM_173717.1:c.2332G>T NP_776065.1:p.Glu778Ter
XM_024450850.1:c.2494G>T XP_024306618.1:p.Glu832Ter
XM_024450851.1:c.2416G>T XP_024306619.1:p.Glu806Ter
XM_024450852.1:c.2413G>T XP_024306620.1:p.Glu805Ter
XM_024450853.1:c.2410G>T XP_024306621.1:p.Glu804Ter
XM_024450854.1:c.2374G>T XP_024306622.1:p.Glu792Ter
XM_024450855.1:c.2293G>T XP_024306623.1:p.Glu765Ter
XM_024450856.1:c.2212G>T XP_024306624.1:p.Glu738Ter
XM_024450857.1:c.2212G>T XP_024306625.1:p.Glu738Ter
XM_024450858.1:c.2131G>T XP_024306626.1:p.Glu711Ter
XM_024450859.1:c.2128G>T XP_024306627.1:p.Glu710Ter
XM_024450860.1:c.2053G>T XP_024306628.1:p.Glu685Ter
XM_024450861.1:c.2053G>T XP_024306629.1:p.Glu685Ter
XM_024450862.1:c.2050G>T XP_024306630.1:p.Glu684Ter
NM_018127.7:c.2335G>T MANE Select NP_060597.4:p.Glu779Ter
NM_001165962.2:c.2215G>T NP_001159434.1:p.Glu739Ter
NM_173717.2:c.2332G>T NP_776065.1:p.Glu778Ter