Canonical Allele Identifier: CA498009628

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896252C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992935C>G , CM000679.2:g.12992935C>G	GRCh38
NC_000017.10:g.12896252C>G , CM000679.1:g.12896252C>G	GRCh37
NC_000017.9:g.12836977C>G	NCBI36
NG_015808.1:g.30130G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2364G>C MANE Select	ENSP00000337445.4:p.Arg788=
ENST00000338034.8:c.2364G>C	ENSP00000337445.4:p.Arg788=
ENST00000395962.6:c.2307G>C	ENSP00000379291.1:p.Arg769=
ENST00000426905.7:c.2244G>C	ENSP00000405223.3:p.Arg748=
ENST00000465825.5:n.2251G>C
ENST00000480891.5:n.2193G>C
ENST00000484122.5:n.3194G>C
ENST00000487229.6:n.1910G>C
ENST00000584650.5:c.1763G>C
NM_001165962.1:c.2244G>C	NP_001159434.1:p.Arg748=
NM_018127.6:c.2364G>C	NP_060597.4:p.Arg788=
NM_173717.1:c.2361G>C	NP_776065.1:p.Arg787=
XM_024450850.1:c.2523G>C	XP_024306618.1:p.Arg841=
XM_024450851.1:c.2445G>C	XP_024306619.1:p.Arg815=
XM_024450852.1:c.2442G>C	XP_024306620.1:p.Arg814=
XM_024450853.1:c.2439G>C	XP_024306621.1:p.Arg813=
XM_024450854.1:c.2403G>C	XP_024306622.1:p.Arg801=
XM_024450855.1:c.2322G>C	XP_024306623.1:p.Arg774=
XM_024450856.1:c.2241G>C	XP_024306624.1:p.Arg747=
XM_024450857.1:c.2241G>C	XP_024306625.1:p.Arg747=
XM_024450858.1:c.2160G>C	XP_024306626.1:p.Arg720=
XM_024450859.1:c.2157G>C	XP_024306627.1:p.Arg719=
XM_024450860.1:c.2082G>C	XP_024306628.1:p.Arg694=
XM_024450861.1:c.2082G>C	XP_024306629.1:p.Arg694=
XM_024450862.1:c.2079G>C	XP_024306630.1:p.Arg693=
NM_018127.7:c.2364G>C MANE Select	NP_060597.4:p.Arg788=
NM_001165962.2:c.2244G>C	NP_001159434.1:p.Arg748=
NM_173717.2:c.2361G>C	NP_776065.1:p.Arg787=