Canonical Allele Identifier: CA498009613

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896234G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992917G>C , CM000679.2:g.12992917G>C	GRCh38
NC_000017.10:g.12896234G>C , CM000679.1:g.12896234G>C	GRCh37
NC_000017.9:g.12836959G>C	NCBI36
NG_015808.1:g.30148C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2382C>G MANE Select	ENSP00000337445.4:p.Leu794=
ENST00000338034.8:c.2382C>G	ENSP00000337445.4:p.Leu794=
ENST00000395962.6:c.2325C>G	ENSP00000379291.1:p.Leu775=
ENST00000426905.7:c.2262C>G	ENSP00000405223.3:p.Leu754=
ENST00000465825.5:n.2269C>G
ENST00000480891.5:n.2211C>G
ENST00000484122.5:n.3212C>G
ENST00000487229.6:n.1928C>G
ENST00000584650.5:c.1781C>G
NM_001165962.1:c.2262C>G	NP_001159434.1:p.Leu754=
NM_018127.6:c.2382C>G	NP_060597.4:p.Leu794=
NM_173717.1:c.2379C>G	NP_776065.1:p.Leu793=
XM_024450850.1:c.2541C>G	XP_024306618.1:p.Leu847=
XM_024450851.1:c.2463C>G	XP_024306619.1:p.Leu821=
XM_024450852.1:c.2460C>G	XP_024306620.1:p.Leu820=
XM_024450853.1:c.2457C>G	XP_024306621.1:p.Leu819=
XM_024450854.1:c.2421C>G	XP_024306622.1:p.Leu807=
XM_024450855.1:c.2340C>G	XP_024306623.1:p.Leu780=
XM_024450856.1:c.2259C>G	XP_024306624.1:p.Leu753=
XM_024450857.1:c.2259C>G	XP_024306625.1:p.Leu753=
XM_024450858.1:c.2178C>G	XP_024306626.1:p.Leu726=
XM_024450859.1:c.2175C>G	XP_024306627.1:p.Leu725=
XM_024450860.1:c.2100C>G	XP_024306628.1:p.Leu700=
XM_024450861.1:c.2100C>G	XP_024306629.1:p.Leu700=
XM_024450862.1:c.2097C>G	XP_024306630.1:p.Leu699=
NM_018127.7:c.2382C>G MANE Select	NP_060597.4:p.Leu794=
NM_001165962.2:c.2262C>G	NP_001159434.1:p.Leu754=
NM_173717.2:c.2379C>G	NP_776065.1:p.Leu793=