Canonical Allele Identifier: CA498009559
Gene: ELAC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.12896153C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.12992836C>T , CM000679.2:g.12992836C>T GRCh38
NC_000017.10:g.12896153C>T , CM000679.1:g.12896153C>T GRCh37
NC_000017.9:g.12836878C>T NCBI36
NG_015808.1:g.30229G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000338034.9:c.2463G>A MANE Select ENSP00000337445.4:p.Lys821=
ENST00000338034.8:c.2463G>A ENSP00000337445.4:p.Lys821=
ENST00000395962.6:c.2406G>A ENSP00000379291.1:p.Lys802=
ENST00000426905.7:c.2343G>A ENSP00000405223.3:p.Lys781=
ENST00000465825.5:n.2350G>A
ENST00000480891.5:n.2292G>A
ENST00000484122.5:n.3293G>A
ENST00000487229.6:n.2009G>A
ENST00000584650.5:c.1862G>A
NM_001165962.1:c.2343G>A NP_001159434.1:p.Lys781=
NM_018127.6:c.2463G>A NP_060597.4:p.Lys821=
NM_173717.1:c.2460G>A NP_776065.1:p.Lys820=
XM_024450850.1:c.2622G>A XP_024306618.1:p.Lys874=
XM_024450851.1:c.2544G>A XP_024306619.1:p.Lys848=
XM_024450852.1:c.2541G>A XP_024306620.1:p.Lys847=
XM_024450853.1:c.2538G>A XP_024306621.1:p.Lys846=
XM_024450854.1:c.2502G>A XP_024306622.1:p.Lys834=
XM_024450855.1:c.2421G>A XP_024306623.1:p.Lys807=
XM_024450856.1:c.2340G>A XP_024306624.1:p.Lys780=
XM_024450857.1:c.2340G>A XP_024306625.1:p.Lys780=
XM_024450858.1:c.2259G>A XP_024306626.1:p.Lys753=
XM_024450859.1:c.2256G>A XP_024306627.1:p.Lys752=
XM_024450860.1:c.2181G>A XP_024306628.1:p.Lys727=
XM_024450861.1:c.2181G>A XP_024306629.1:p.Lys727=
XM_024450862.1:c.2178G>A XP_024306630.1:p.Lys726=
NM_018127.7:c.2463G>A MANE Select NP_060597.4:p.Lys821=
NM_001165962.2:c.2343G>A NP_001159434.1:p.Lys781=
NM_173717.2:c.2460G>A NP_776065.1:p.Lys820=