Canonical Allele Identifier: CA498009622

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896243C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992926C>T , CM000679.2:g.12992926C>T	GRCh38
NC_000017.10:g.12896243C>T , CM000679.1:g.12896243C>T	GRCh37
NC_000017.9:g.12836968C>T	NCBI36
NG_015808.1:g.30139G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2373G>A MANE Select	ENSP00000337445.4:p.Arg791=
ENST00000338034.8:c.2373G>A	ENSP00000337445.4:p.Arg791=
ENST00000395962.6:c.2316G>A	ENSP00000379291.1:p.Arg772=
ENST00000426905.7:c.2253G>A	ENSP00000405223.3:p.Arg751=
ENST00000465825.5:n.2260G>A
ENST00000480891.5:n.2202G>A
ENST00000484122.5:n.3203G>A
ENST00000487229.6:n.1919G>A
ENST00000584650.5:c.1772G>A
NM_001165962.1:c.2253G>A	NP_001159434.1:p.Arg751=
NM_018127.6:c.2373G>A	NP_060597.4:p.Arg791=
NM_173717.1:c.2370G>A	NP_776065.1:p.Arg790=
XM_024450850.1:c.2532G>A	XP_024306618.1:p.Arg844=
XM_024450851.1:c.2454G>A	XP_024306619.1:p.Arg818=
XM_024450852.1:c.2451G>A	XP_024306620.1:p.Arg817=
XM_024450853.1:c.2448G>A	XP_024306621.1:p.Arg816=
XM_024450854.1:c.2412G>A	XP_024306622.1:p.Arg804=
XM_024450855.1:c.2331G>A	XP_024306623.1:p.Arg777=
XM_024450856.1:c.2250G>A	XP_024306624.1:p.Arg750=
XM_024450857.1:c.2250G>A	XP_024306625.1:p.Arg750=
XM_024450858.1:c.2169G>A	XP_024306626.1:p.Arg723=
XM_024450859.1:c.2166G>A	XP_024306627.1:p.Arg722=
XM_024450860.1:c.2091G>A	XP_024306628.1:p.Arg697=
XM_024450861.1:c.2091G>A	XP_024306629.1:p.Arg697=
XM_024450862.1:c.2088G>A	XP_024306630.1:p.Arg696=
NM_018127.7:c.2373G>A MANE Select	NP_060597.4:p.Arg791=
NM_001165962.2:c.2253G>A	NP_001159434.1:p.Arg751=
NM_173717.2:c.2370G>A	NP_776065.1:p.Arg790=