Canonical Allele Identifier: CA398222434
Gene: ELAC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.12993037A>C , CM000679.2:g.12993037A>C GRCh38
NC_000017.10:g.12896354A>C , CM000679.1:g.12896354A>C GRCh37
NC_000017.9:g.12837079A>C NCBI36
NG_015808.1:g.30028T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000338034.9:c.2262T>G MANE Select ENSP00000337445.4:p.Phe754Leu
ENST00000338034.8:c.2262T>G ENSP00000337445.4:p.Phe754Leu
ENST00000395962.6:c.2205T>G ENSP00000379291.1:p.Phe735Leu
ENST00000426905.7:c.2142T>G ENSP00000405223.3:p.Phe714Leu
ENST00000465825.5:n.2149T>G
ENST00000480891.5:n.2091T>G
ENST00000484122.5:n.3092T>G
ENST00000487229.6:n.1808T>G
ENST00000584650.5:c.1661T>G
NM_001165962.1:c.2142T>G NP_001159434.1:p.Phe714Leu
NM_018127.6:c.2262T>G NP_060597.4:p.Phe754Leu
NM_173717.1:c.2259T>G NP_776065.1:p.Phe753Leu
XM_024450850.1:c.2421T>G XP_024306618.1:p.Phe807Leu
XM_024450851.1:c.2343T>G XP_024306619.1:p.Phe781Leu
XM_024450852.1:c.2340T>G XP_024306620.1:p.Phe780Leu
XM_024450853.1:c.2337T>G XP_024306621.1:p.Phe779Leu
XM_024450854.1:c.2301T>G XP_024306622.1:p.Phe767Leu
XM_024450855.1:c.2220T>G XP_024306623.1:p.Phe740Leu
XM_024450856.1:c.2139T>G XP_024306624.1:p.Phe713Leu
XM_024450857.1:c.2139T>G XP_024306625.1:p.Phe713Leu
XM_024450858.1:c.2058T>G XP_024306626.1:p.Phe686Leu
XM_024450859.1:c.2055T>G XP_024306627.1:p.Phe685Leu
XM_024450860.1:c.1980T>G XP_024306628.1:p.Phe660Leu
XM_024450861.1:c.1980T>G XP_024306629.1:p.Phe660Leu
XM_024450862.1:c.1977T>G XP_024306630.1:p.Phe659Leu
NM_018127.7:c.2262T>G MANE Select NP_060597.4:p.Phe754Leu
NM_001165962.2:c.2142T>G NP_001159434.1:p.Phe714Leu
NM_173717.2:c.2259T>G NP_776065.1:p.Phe753Leu