Canonical Allele Identifier: CA398222299

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896288C>A (hg19) ; chr17:g.12992971C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992971C>A , CM000679.2:g.12992971C>A	GRCh38
NC_000017.10:g.12896288C>A , CM000679.1:g.12896288C>A	GRCh37
NC_000017.9:g.12837013C>A	NCBI36
NG_015808.1:g.30094G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2328G>T MANE Select	ENSP00000337445.4:p.Glu776Asp
ENST00000338034.8:c.2328G>T	ENSP00000337445.4:p.Glu776Asp
ENST00000395962.6:c.2271G>T	ENSP00000379291.1:p.Glu757Asp
ENST00000426905.7:c.2208G>T	ENSP00000405223.3:p.Glu736Asp
ENST00000465825.5:n.2215G>T
ENST00000480891.5:n.2157G>T
ENST00000484122.5:n.3158G>T
ENST00000487229.6:n.1874G>T
ENST00000584650.5:c.1727G>T
NM_001165962.1:c.2208G>T	NP_001159434.1:p.Glu736Asp
NM_018127.6:c.2328G>T	NP_060597.4:p.Glu776Asp
NM_173717.1:c.2325G>T	NP_776065.1:p.Glu775Asp
XM_024450850.1:c.2487G>T	XP_024306618.1:p.Glu829Asp
XM_024450851.1:c.2409G>T	XP_024306619.1:p.Glu803Asp
XM_024450852.1:c.2406G>T	XP_024306620.1:p.Glu802Asp
XM_024450853.1:c.2403G>T	XP_024306621.1:p.Glu801Asp
XM_024450854.1:c.2367G>T	XP_024306622.1:p.Glu789Asp
XM_024450855.1:c.2286G>T	XP_024306623.1:p.Glu762Asp
XM_024450856.1:c.2205G>T	XP_024306624.1:p.Glu735Asp
XM_024450857.1:c.2205G>T	XP_024306625.1:p.Glu735Asp
XM_024450858.1:c.2124G>T	XP_024306626.1:p.Glu708Asp
XM_024450859.1:c.2121G>T	XP_024306627.1:p.Glu707Asp
XM_024450860.1:c.2046G>T	XP_024306628.1:p.Glu682Asp
XM_024450861.1:c.2046G>T	XP_024306629.1:p.Glu682Asp
XM_024450862.1:c.2043G>T	XP_024306630.1:p.Glu681Asp
NM_018127.7:c.2328G>T MANE Select	NP_060597.4:p.Glu776Asp
NM_001165962.2:c.2208G>T	NP_001159434.1:p.Glu736Asp
NM_173717.2:c.2325G>T	NP_776065.1:p.Glu775Asp