Canonical Allele Identifier: CA398222436

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896355A>C (hg19) ; chr17:g.12993038A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12993038A>C , CM000679.2:g.12993038A>C	GRCh38
NC_000017.10:g.12896355A>C , CM000679.1:g.12896355A>C	GRCh37
NC_000017.9:g.12837080A>C	NCBI36
NG_015808.1:g.30027T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2261T>G MANE Select	ENSP00000337445.4:p.Phe754Cys
ENST00000338034.8:c.2261T>G	ENSP00000337445.4:p.Phe754Cys
ENST00000395962.6:c.2204T>G	ENSP00000379291.1:p.Phe735Cys
ENST00000426905.7:c.2141T>G	ENSP00000405223.3:p.Phe714Cys
ENST00000465825.5:n.2148T>G
ENST00000480891.5:n.2090T>G
ENST00000484122.5:n.3091T>G
ENST00000487229.6:n.1807T>G
ENST00000584650.5:c.1660T>G
NM_001165962.1:c.2141T>G	NP_001159434.1:p.Phe714Cys
NM_018127.6:c.2261T>G	NP_060597.4:p.Phe754Cys
NM_173717.1:c.2258T>G	NP_776065.1:p.Phe753Cys
XM_024450850.1:c.2420T>G	XP_024306618.1:p.Phe807Cys
XM_024450851.1:c.2342T>G	XP_024306619.1:p.Phe781Cys
XM_024450852.1:c.2339T>G	XP_024306620.1:p.Phe780Cys
XM_024450853.1:c.2336T>G	XP_024306621.1:p.Phe779Cys
XM_024450854.1:c.2300T>G	XP_024306622.1:p.Phe767Cys
XM_024450855.1:c.2219T>G	XP_024306623.1:p.Phe740Cys
XM_024450856.1:c.2138T>G	XP_024306624.1:p.Phe713Cys
XM_024450857.1:c.2138T>G	XP_024306625.1:p.Phe713Cys
XM_024450858.1:c.2057T>G	XP_024306626.1:p.Phe686Cys
XM_024450859.1:c.2054T>G	XP_024306627.1:p.Phe685Cys
XM_024450860.1:c.1979T>G	XP_024306628.1:p.Phe660Cys
XM_024450861.1:c.1979T>G	XP_024306629.1:p.Phe660Cys
XM_024450862.1:c.1976T>G	XP_024306630.1:p.Phe659Cys
NM_018127.7:c.2261T>G MANE Select	NP_060597.4:p.Phe754Cys
NM_001165962.2:c.2141T>G	NP_001159434.1:p.Phe714Cys
NM_173717.2:c.2258T>G	NP_776065.1:p.Phe753Cys