Canonical Allele Identifier: CA498009586

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896198C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992881C>A , CM000679.2:g.12992881C>A	GRCh38
NC_000017.10:g.12896198C>A , CM000679.1:g.12896198C>A	GRCh37
NC_000017.9:g.12836923C>A	NCBI36
NG_015808.1:g.30184G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2418G>T MANE Select	ENSP00000337445.4:p.Gly806=
ENST00000338034.8:c.2418G>T	ENSP00000337445.4:p.Gly806=
ENST00000395962.6:c.2361G>T	ENSP00000379291.1:p.Gly787=
ENST00000426905.7:c.2298G>T	ENSP00000405223.3:p.Gly766=
ENST00000465825.5:n.2305G>T
ENST00000480891.5:n.2247G>T
ENST00000484122.5:n.3248G>T
ENST00000487229.6:n.1964G>T
ENST00000584650.5:c.1817G>T
NM_001165962.1:c.2298G>T	NP_001159434.1:p.Gly766=
NM_018127.6:c.2418G>T	NP_060597.4:p.Gly806=
NM_173717.1:c.2415G>T	NP_776065.1:p.Gly805=
XM_024450850.1:c.2577G>T	XP_024306618.1:p.Gly859=
XM_024450851.1:c.2499G>T	XP_024306619.1:p.Gly833=
XM_024450852.1:c.2496G>T	XP_024306620.1:p.Gly832=
XM_024450853.1:c.2493G>T	XP_024306621.1:p.Gly831=
XM_024450854.1:c.2457G>T	XP_024306622.1:p.Gly819=
XM_024450855.1:c.2376G>T	XP_024306623.1:p.Gly792=
XM_024450856.1:c.2295G>T	XP_024306624.1:p.Gly765=
XM_024450857.1:c.2295G>T	XP_024306625.1:p.Gly765=
XM_024450858.1:c.2214G>T	XP_024306626.1:p.Gly738=
XM_024450859.1:c.2211G>T	XP_024306627.1:p.Gly737=
XM_024450860.1:c.2136G>T	XP_024306628.1:p.Gly712=
XM_024450861.1:c.2136G>T	XP_024306629.1:p.Gly712=
XM_024450862.1:c.2133G>T	XP_024306630.1:p.Gly711=
NM_018127.7:c.2418G>T MANE Select	NP_060597.4:p.Gly806=
NM_001165962.2:c.2298G>T	NP_001159434.1:p.Gly766=
NM_173717.2:c.2415G>T	NP_776065.1:p.Gly805=