Canonical Allele Identifier: CA398222094
Gene: ELAC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.12992867T>A , CM000679.2:g.12992867T>A GRCh38
NC_000017.10:g.12896184T>A , CM000679.1:g.12896184T>A GRCh37
NC_000017.9:g.12836909T>A NCBI36
NG_015808.1:g.30198A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000338034.9:c.2432A>T MANE Select ENSP00000337445.4:p.Lys811Met
ENST00000338034.8:c.2432A>T ENSP00000337445.4:p.Lys811Met
ENST00000395962.6:c.2375A>T ENSP00000379291.1:p.Lys792Met
ENST00000426905.7:c.2312A>T ENSP00000405223.3:p.Lys771Met
ENST00000465825.5:n.2319A>T
ENST00000480891.5:n.2261A>T
ENST00000484122.5:n.3262A>T
ENST00000487229.6:n.1978A>T
ENST00000584650.5:c.1831A>T
NM_001165962.1:c.2312A>T NP_001159434.1:p.Lys771Met
NM_018127.6:c.2432A>T NP_060597.4:p.Lys811Met
NM_173717.1:c.2429A>T NP_776065.1:p.Lys810Met
XM_024450850.1:c.2591A>T XP_024306618.1:p.Lys864Met
XM_024450851.1:c.2513A>T XP_024306619.1:p.Lys838Met
XM_024450852.1:c.2510A>T XP_024306620.1:p.Lys837Met
XM_024450853.1:c.2507A>T XP_024306621.1:p.Lys836Met
XM_024450854.1:c.2471A>T XP_024306622.1:p.Lys824Met
XM_024450855.1:c.2390A>T XP_024306623.1:p.Lys797Met
XM_024450856.1:c.2309A>T XP_024306624.1:p.Lys770Met
XM_024450857.1:c.2309A>T XP_024306625.1:p.Lys770Met
XM_024450858.1:c.2228A>T XP_024306626.1:p.Lys743Met
XM_024450859.1:c.2225A>T XP_024306627.1:p.Lys742Met
XM_024450860.1:c.2150A>T XP_024306628.1:p.Lys717Met
XM_024450861.1:c.2150A>T XP_024306629.1:p.Lys717Met
XM_024450862.1:c.2147A>T XP_024306630.1:p.Lys716Met
NM_018127.7:c.2432A>T MANE Select NP_060597.4:p.Lys811Met
NM_001165962.2:c.2312A>T NP_001159434.1:p.Lys771Met
NM_173717.2:c.2429A>T NP_776065.1:p.Lys810Met