Canonical Allele Identifier: CA398222141

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896205T>A (hg19) ; chr17:g.12992888T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992888T>A , CM000679.2:g.12992888T>A	GRCh38
NC_000017.10:g.12896205T>A , CM000679.1:g.12896205T>A	GRCh37
NC_000017.9:g.12836930T>A	NCBI36
NG_015808.1:g.30177A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2411A>T MANE Select	ENSP00000337445.4:p.Glu804Val
ENST00000338034.8:c.2411A>T	ENSP00000337445.4:p.Glu804Val
ENST00000395962.6:c.2354A>T	ENSP00000379291.1:p.Glu785Val
ENST00000426905.7:c.2291A>T	ENSP00000405223.3:p.Glu764Val
ENST00000465825.5:n.2298A>T
ENST00000480891.5:n.2240A>T
ENST00000484122.5:n.3241A>T
ENST00000487229.6:n.1957A>T
ENST00000584650.5:c.1810A>T
NM_001165962.1:c.2291A>T	NP_001159434.1:p.Glu764Val
NM_018127.6:c.2411A>T	NP_060597.4:p.Glu804Val
NM_173717.1:c.2408A>T	NP_776065.1:p.Glu803Val
XM_024450850.1:c.2570A>T	XP_024306618.1:p.Glu857Val
XM_024450851.1:c.2492A>T	XP_024306619.1:p.Glu831Val
XM_024450852.1:c.2489A>T	XP_024306620.1:p.Glu830Val
XM_024450853.1:c.2486A>T	XP_024306621.1:p.Glu829Val
XM_024450854.1:c.2450A>T	XP_024306622.1:p.Glu817Val
XM_024450855.1:c.2369A>T	XP_024306623.1:p.Glu790Val
XM_024450856.1:c.2288A>T	XP_024306624.1:p.Glu763Val
XM_024450857.1:c.2288A>T	XP_024306625.1:p.Glu763Val
XM_024450858.1:c.2207A>T	XP_024306626.1:p.Glu736Val
XM_024450859.1:c.2204A>T	XP_024306627.1:p.Glu735Val
XM_024450860.1:c.2129A>T	XP_024306628.1:p.Glu710Val
XM_024450861.1:c.2129A>T	XP_024306629.1:p.Glu710Val
XM_024450862.1:c.2126A>T	XP_024306630.1:p.Glu709Val
NM_018127.7:c.2411A>T MANE Select	NP_060597.4:p.Glu804Val
NM_001165962.2:c.2291A>T	NP_001159434.1:p.Glu764Val
NM_173717.2:c.2408A>T	NP_776065.1:p.Glu803Val