Canonical Allele Identifier: CA2248421214

Gene: ELAC2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992779A= , CM000679.2:g.12992779A=	GRCh38
NC_000017.10:g.12896096A= , CM000679.1:g.12896096A=	GRCh37
NC_000017.9:g.12836821A=	NCBI36
NG_015808.1:g.30286T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000338034.9:c.*39T= MANE Select	ENSP00000337445.4:n.*39T=
ENST00000338034.8:c.*39T=	ENSP00000337445.4:n.*39T=
ENST00000395962.6:c.*39T=	ENSP00000379291.1:n.*39T=
ENST00000426905.7:c.*39T=	ENSP00000405223.3:n.*39T=
ENST00000465825.5:n.2407T=
ENST00000480891.5:n.2349T=
ENST00000484122.5:n.3350T=
ENST00000487229.6:n.2066T=
ENST00000584650.5:c.1919T=
NM_001165962.1:c.*39T=	NP_001159434.1:n.*39T=
NM_018127.6:c.*39T=	NP_060597.4:n.*39T=
NM_173717.1:c.*39T=	NP_776065.1:n.*39T=
XM_024450850.1:c.*39T=	XP_024306618.1:n.*39T=
XM_024450851.1:c.*39T=	XP_024306619.1:n.*39T=
XM_024450852.1:c.*39T=	XP_024306620.1:n.*39T=
XM_024450853.1:c.*39T=	XP_024306621.1:n.*39T=
XM_024450854.1:c.*39T=	XP_024306622.1:n.*39T=
XM_024450855.1:c.*39T=	XP_024306623.1:n.*39T=
XM_024450856.1:c.*39T=	XP_024306624.1:n.*39T=
XM_024450857.1:c.*39T=	XP_024306625.1:n.*39T=
XM_024450858.1:c.*39T=	XP_024306626.1:n.*39T=
XM_024450859.1:c.*39T=	XP_024306627.1:n.*39T=
XM_024450860.1:c.*39T=	XP_024306628.1:n.*39T=
XM_024450861.1:c.*39T=	XP_024306629.1:n.*39T=
XM_024450862.1:c.*39T=	XP_024306630.1:n.*39T=
NM_018127.7:c.*39T= MANE Select	NP_060597.4:n.*39T=
NM_001165962.2:c.*39T=	NP_001159434.1:n.*39T=
NM_173717.2:c.*39T=	NP_776065.1:n.*39T=