Canonical Allele Identifier: CA2248421505

Gene: ELAC2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992915A= , CM000679.2:g.12992915A=	GRCh38
NC_000017.10:g.12896232A= , CM000679.1:g.12896232A=	GRCh37
NC_000017.9:g.12836957A=	NCBI36
NG_015808.1:g.30150T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2384T= MANE Select	ENSP00000337445.4:p.Leu795=
ENST00000338034.8:c.2384T=	ENSP00000337445.4:p.Leu795=
ENST00000395962.6:c.2327T=	ENSP00000379291.1:p.Leu776=
ENST00000426905.7:c.2264T=	ENSP00000405223.3:p.Leu755=
ENST00000465825.5:n.2271T=
ENST00000480891.5:n.2213T=
ENST00000484122.5:n.3214T=
ENST00000487229.6:n.1930T=
ENST00000584650.5:c.1783T=
NM_001165962.1:c.2264T=	NP_001159434.1:p.Leu755=
NM_018127.6:c.2384T=	NP_060597.4:p.Leu795=
NM_173717.1:c.2381T=	NP_776065.1:p.Leu794=
XM_024450850.1:c.2543T=	XP_024306618.1:p.Leu848=
XM_024450851.1:c.2465T=	XP_024306619.1:p.Leu822=
XM_024450852.1:c.2462T=	XP_024306620.1:p.Leu821=
XM_024450853.1:c.2459T=	XP_024306621.1:p.Leu820=
XM_024450854.1:c.2423T=	XP_024306622.1:p.Leu808=
XM_024450855.1:c.2342T=	XP_024306623.1:p.Leu781=
XM_024450856.1:c.2261T=	XP_024306624.1:p.Leu754=
XM_024450857.1:c.2261T=	XP_024306625.1:p.Leu754=
XM_024450858.1:c.2180T=	XP_024306626.1:p.Leu727=
XM_024450859.1:c.2177T=	XP_024306627.1:p.Leu726=
XM_024450860.1:c.2102T=	XP_024306628.1:p.Leu701=
XM_024450861.1:c.2102T=	XP_024306629.1:p.Leu701=
XM_024450862.1:c.2099T=	XP_024306630.1:p.Leu700=
NM_018127.7:c.2384T= MANE Select	NP_060597.4:p.Leu795=
NM_001165962.2:c.2264T=	NP_001159434.1:p.Leu755=
NM_173717.2:c.2381T=	NP_776065.1:p.Leu794=