Canonical Allele Identifier: CA2248421758

Gene: ELAC2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12993019C= , CM000679.2:g.12993019C=	GRCh38
NC_000017.10:g.12896336C= , CM000679.1:g.12896336C=	GRCh37
NC_000017.9:g.12837061C=	NCBI36
NG_015808.1:g.30046G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2280G= MANE Select	ENSP00000337445.4:p.Met760=
ENST00000338034.8:c.2280G=	ENSP00000337445.4:p.Met760=
ENST00000395962.6:c.2223G=	ENSP00000379291.1:p.Met741=
ENST00000426905.7:c.2160G=	ENSP00000405223.3:p.Met720=
ENST00000465825.5:n.2167G=
ENST00000480891.5:n.2109G=
ENST00000484122.5:n.3110G=
ENST00000487229.6:n.1826G=
ENST00000584650.5:c.1679G=
NM_001165962.1:c.2160G=	NP_001159434.1:p.Met720=
NM_018127.6:c.2280G=	NP_060597.4:p.Met760=
NM_173717.1:c.2277G=	NP_776065.1:p.Met759=
XM_024450850.1:c.2439G=	XP_024306618.1:p.Met813=
XM_024450851.1:c.2361G=	XP_024306619.1:p.Met787=
XM_024450852.1:c.2358G=	XP_024306620.1:p.Met786=
XM_024450853.1:c.2355G=	XP_024306621.1:p.Met785=
XM_024450854.1:c.2319G=	XP_024306622.1:p.Met773=
XM_024450855.1:c.2238G=	XP_024306623.1:p.Met746=
XM_024450856.1:c.2157G=	XP_024306624.1:p.Met719=
XM_024450857.1:c.2157G=	XP_024306625.1:p.Met719=
XM_024450858.1:c.2076G=	XP_024306626.1:p.Met692=
XM_024450859.1:c.2073G=	XP_024306627.1:p.Met691=
XM_024450860.1:c.1998G=	XP_024306628.1:p.Met666=
XM_024450861.1:c.1998G=	XP_024306629.1:p.Met666=
XM_024450862.1:c.1995G=	XP_024306630.1:p.Met665=
NM_018127.7:c.2280G= MANE Select	NP_060597.4:p.Met760=
NM_001165962.2:c.2160G=	NP_001159434.1:p.Met720=
NM_173717.2:c.2277G=	NP_776065.1:p.Met759=