Canonical Allele Identifier: CA498009602

Gene: ELAC2

Linked Data

• gnomAD v4: 17-12992905-C-T
• MyVariant Identifiers: chr17:g.12896222C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992905C>T , CM000679.2:g.12992905C>T	GRCh38
NC_000017.10:g.12896222C>T , CM000679.1:g.12896222C>T	GRCh37
NC_000017.9:g.12836947C>T	NCBI36
NG_015808.1:g.30160G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2394G>A MANE Select	ENSP00000337445.4:p.Glu798=
ENST00000338034.8:c.2394G>A	ENSP00000337445.4:p.Glu798=
ENST00000395962.6:c.2337G>A	ENSP00000379291.1:p.Glu779=
ENST00000426905.7:c.2274G>A	ENSP00000405223.3:p.Glu758=
ENST00000465825.5:n.2281G>A
ENST00000480891.5:n.2223G>A
ENST00000484122.5:n.3224G>A
ENST00000487229.6:n.1940G>A
ENST00000584650.5:c.1793G>A
NM_001165962.1:c.2274G>A	NP_001159434.1:p.Glu758=
NM_018127.6:c.2394G>A	NP_060597.4:p.Glu798=
NM_173717.1:c.2391G>A	NP_776065.1:p.Glu797=
XM_024450850.1:c.2553G>A	XP_024306618.1:p.Glu851=
XM_024450851.1:c.2475G>A	XP_024306619.1:p.Glu825=
XM_024450852.1:c.2472G>A	XP_024306620.1:p.Glu824=
XM_024450853.1:c.2469G>A	XP_024306621.1:p.Glu823=
XM_024450854.1:c.2433G>A	XP_024306622.1:p.Glu811=
XM_024450855.1:c.2352G>A	XP_024306623.1:p.Glu784=
XM_024450856.1:c.2271G>A	XP_024306624.1:p.Glu757=
XM_024450857.1:c.2271G>A	XP_024306625.1:p.Glu757=
XM_024450858.1:c.2190G>A	XP_024306626.1:p.Glu730=
XM_024450859.1:c.2187G>A	XP_024306627.1:p.Glu729=
XM_024450860.1:c.2112G>A	XP_024306628.1:p.Glu704=
XM_024450861.1:c.2112G>A	XP_024306629.1:p.Glu704=
XM_024450862.1:c.2109G>A	XP_024306630.1:p.Glu703=
NM_018127.7:c.2394G>A MANE Select	NP_060597.4:p.Glu798=
NM_001165962.2:c.2274G>A	NP_001159434.1:p.Glu758=
NM_173717.2:c.2391G>A	NP_776065.1:p.Glu797=