Canonical Allele Identifier: CA498009650

Gene: ELAC2

Linked Data

• COSMIC: COSM4680695
• MyVariant Identifiers: chr17:g.12896279C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992962C>T , CM000679.2:g.12992962C>T	GRCh38
NC_000017.10:g.12896279C>T , CM000679.1:g.12896279C>T	GRCh37
NC_000017.9:g.12837004C>T	NCBI36
NG_015808.1:g.30103G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000338034.9:c.2337G>A MANE Select	ENSP00000337445.4:p.Glu779=
ENST00000338034.8:c.2337G>A	ENSP00000337445.4:p.Glu779=
ENST00000395962.6:c.2280G>A	ENSP00000379291.1:p.Glu760=
ENST00000426905.7:c.2217G>A	ENSP00000405223.3:p.Glu739=
ENST00000465825.5:n.2224G>A
ENST00000480891.5:n.2166G>A
ENST00000484122.5:n.3167G>A
ENST00000487229.6:n.1883G>A
ENST00000584650.5:c.1736G>A
NM_001165962.1:c.2217G>A	NP_001159434.1:p.Glu739=
NM_018127.6:c.2337G>A	NP_060597.4:p.Glu779=
NM_173717.1:c.2334G>A	NP_776065.1:p.Glu778=
XM_024450850.1:c.2496G>A	XP_024306618.1:p.Glu832=
XM_024450851.1:c.2418G>A	XP_024306619.1:p.Glu806=
XM_024450852.1:c.2415G>A	XP_024306620.1:p.Glu805=
XM_024450853.1:c.2412G>A	XP_024306621.1:p.Glu804=
XM_024450854.1:c.2376G>A	XP_024306622.1:p.Glu792=
XM_024450855.1:c.2295G>A	XP_024306623.1:p.Glu765=
XM_024450856.1:c.2214G>A	XP_024306624.1:p.Glu738=
XM_024450857.1:c.2214G>A	XP_024306625.1:p.Glu738=
XM_024450858.1:c.2133G>A	XP_024306626.1:p.Glu711=
XM_024450859.1:c.2130G>A	XP_024306627.1:p.Glu710=
XM_024450860.1:c.2055G>A	XP_024306628.1:p.Glu685=
XM_024450861.1:c.2055G>A	XP_024306629.1:p.Glu685=
XM_024450862.1:c.2052G>A	XP_024306630.1:p.Glu684=
NM_018127.7:c.2337G>A MANE Select	NP_060597.4:p.Glu779=
NM_001165962.2:c.2217G>A	NP_001159434.1:p.Glu739=
NM_173717.2:c.2334G>A	NP_776065.1:p.Glu778=