Canonical Allele Identifier: CA398222031
Gene: ELAC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.12992837T>C , CM000679.2:g.12992837T>C GRCh38
NC_000017.10:g.12896154T>C , CM000679.1:g.12896154T>C GRCh37
NC_000017.9:g.12836879T>C NCBI36
NG_015808.1:g.30228A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338034.9:c.2462A>G MANE Select ENSP00000337445.4:p.Lys821Arg
ENST00000338034.8:c.2462A>G ENSP00000337445.4:p.Lys821Arg
ENST00000395962.6:c.2405A>G ENSP00000379291.1:p.Lys802Arg
ENST00000426905.7:c.2342A>G ENSP00000405223.3:p.Lys781Arg
ENST00000465825.5:n.2349A>G
ENST00000480891.5:n.2291A>G
ENST00000484122.5:n.3292A>G
ENST00000487229.6:n.2008A>G
ENST00000584650.5:c.1861A>G
NM_001165962.1:c.2342A>G NP_001159434.1:p.Lys781Arg
NM_018127.6:c.2462A>G NP_060597.4:p.Lys821Arg
NM_173717.1:c.2459A>G NP_776065.1:p.Lys820Arg
XM_024450850.1:c.2621A>G XP_024306618.1:p.Lys874Arg
XM_024450851.1:c.2543A>G XP_024306619.1:p.Lys848Arg
XM_024450852.1:c.2540A>G XP_024306620.1:p.Lys847Arg
XM_024450853.1:c.2537A>G XP_024306621.1:p.Lys846Arg
XM_024450854.1:c.2501A>G XP_024306622.1:p.Lys834Arg
XM_024450855.1:c.2420A>G XP_024306623.1:p.Lys807Arg
XM_024450856.1:c.2339A>G XP_024306624.1:p.Lys780Arg
XM_024450857.1:c.2339A>G XP_024306625.1:p.Lys780Arg
XM_024450858.1:c.2258A>G XP_024306626.1:p.Lys753Arg
XM_024450859.1:c.2255A>G XP_024306627.1:p.Lys752Arg
XM_024450860.1:c.2180A>G XP_024306628.1:p.Lys727Arg
XM_024450861.1:c.2180A>G XP_024306629.1:p.Lys727Arg
XM_024450862.1:c.2177A>G XP_024306630.1:p.Lys726Arg
NM_018127.7:c.2462A>G MANE Select NP_060597.4:p.Lys821Arg
NM_001165962.2:c.2342A>G NP_001159434.1:p.Lys781Arg
NM_173717.2:c.2459A>G NP_776065.1:p.Lys820Arg