Canonical Allele Identifier: CA2248421731

Gene: ELAC2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12993004G= , CM000679.2:g.12993004G=	GRCh38
NC_000017.10:g.12896321G= , CM000679.1:g.12896321G=	GRCh37
NC_000017.9:g.12837046G=	NCBI36
NG_015808.1:g.30061C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2295C= MANE Select	ENSP00000337445.4:p.Pro765=
ENST00000338034.8:c.2295C=	ENSP00000337445.4:p.Pro765=
ENST00000395962.6:c.2238C=	ENSP00000379291.1:p.Pro746=
ENST00000426905.7:c.2175C=	ENSP00000405223.3:p.Pro725=
ENST00000465825.5:n.2182C=
ENST00000480891.5:n.2124C=
ENST00000484122.5:n.3125C=
ENST00000487229.6:n.1841C=
ENST00000584650.5:c.1694C=
NM_001165962.1:c.2175C=	NP_001159434.1:p.Pro725=
NM_018127.6:c.2295C=	NP_060597.4:p.Pro765=
NM_173717.1:c.2292C=	NP_776065.1:p.Pro764=
XM_024450850.1:c.2454C=	XP_024306618.1:p.Pro818=
XM_024450851.1:c.2376C=	XP_024306619.1:p.Pro792=
XM_024450852.1:c.2373C=	XP_024306620.1:p.Pro791=
XM_024450853.1:c.2370C=	XP_024306621.1:p.Pro790=
XM_024450854.1:c.2334C=	XP_024306622.1:p.Pro778=
XM_024450855.1:c.2253C=	XP_024306623.1:p.Pro751=
XM_024450856.1:c.2172C=	XP_024306624.1:p.Pro724=
XM_024450857.1:c.2172C=	XP_024306625.1:p.Pro724=
XM_024450858.1:c.2091C=	XP_024306626.1:p.Pro697=
XM_024450859.1:c.2088C=	XP_024306627.1:p.Pro696=
XM_024450860.1:c.2013C=	XP_024306628.1:p.Pro671=
XM_024450861.1:c.2013C=	XP_024306629.1:p.Pro671=
XM_024450862.1:c.2010C=	XP_024306630.1:p.Pro670=
NM_018127.7:c.2295C= MANE Select	NP_060597.4:p.Pro765=
NM_001165962.2:c.2175C=	NP_001159434.1:p.Pro725=
NM_173717.2:c.2292C=	NP_776065.1:p.Pro764=