Canonical Allele Identifier: CA398222413

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896345A>C (hg19) ; chr17:g.12993028A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12993028A>C , CM000679.2:g.12993028A>C	GRCh38
NC_000017.10:g.12896345A>C , CM000679.1:g.12896345A>C	GRCh37
NC_000017.9:g.12837070A>C	NCBI36
NG_015808.1:g.30037T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2271T>G MANE Select	ENSP00000337445.4:p.Phe757Leu
ENST00000338034.8:c.2271T>G	ENSP00000337445.4:p.Phe757Leu
ENST00000395962.6:c.2214T>G	ENSP00000379291.1:p.Phe738Leu
ENST00000426905.7:c.2151T>G	ENSP00000405223.3:p.Phe717Leu
ENST00000465825.5:n.2158T>G
ENST00000480891.5:n.2100T>G
ENST00000484122.5:n.3101T>G
ENST00000487229.6:n.1817T>G
ENST00000584650.5:c.1670T>G
NM_001165962.1:c.2151T>G	NP_001159434.1:p.Phe717Leu
NM_018127.6:c.2271T>G	NP_060597.4:p.Phe757Leu
NM_173717.1:c.2268T>G	NP_776065.1:p.Phe756Leu
XM_024450850.1:c.2430T>G	XP_024306618.1:p.Phe810Leu
XM_024450851.1:c.2352T>G	XP_024306619.1:p.Phe784Leu
XM_024450852.1:c.2349T>G	XP_024306620.1:p.Phe783Leu
XM_024450853.1:c.2346T>G	XP_024306621.1:p.Phe782Leu
XM_024450854.1:c.2310T>G	XP_024306622.1:p.Phe770Leu
XM_024450855.1:c.2229T>G	XP_024306623.1:p.Phe743Leu
XM_024450856.1:c.2148T>G	XP_024306624.1:p.Phe716Leu
XM_024450857.1:c.2148T>G	XP_024306625.1:p.Phe716Leu
XM_024450858.1:c.2067T>G	XP_024306626.1:p.Phe689Leu
XM_024450859.1:c.2064T>G	XP_024306627.1:p.Phe688Leu
XM_024450860.1:c.1989T>G	XP_024306628.1:p.Phe663Leu
XM_024450861.1:c.1989T>G	XP_024306629.1:p.Phe663Leu
XM_024450862.1:c.1986T>G	XP_024306630.1:p.Phe662Leu
NM_018127.7:c.2271T>G MANE Select	NP_060597.4:p.Phe757Leu
NM_001165962.2:c.2151T>G	NP_001159434.1:p.Phe717Leu
NM_173717.2:c.2268T>G	NP_776065.1:p.Phe756Leu