Canonical Allele Identifier: CA398222135

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896202T>G (hg19) ; chr17:g.12992885T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992885T>G , CM000679.2:g.12992885T>G	GRCh38
NC_000017.10:g.12896202T>G , CM000679.1:g.12896202T>G	GRCh37
NC_000017.9:g.12836927T>G	NCBI36
NG_015808.1:g.30180A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2414A>C MANE Select	ENSP00000337445.4:p.Asp805Ala
ENST00000338034.8:c.2414A>C	ENSP00000337445.4:p.Asp805Ala
ENST00000395962.6:c.2357A>C	ENSP00000379291.1:p.Asp786Ala
ENST00000426905.7:c.2294A>C	ENSP00000405223.3:p.Asp765Ala
ENST00000465825.5:n.2301A>C
ENST00000480891.5:n.2243A>C
ENST00000484122.5:n.3244A>C
ENST00000487229.6:n.1960A>C
ENST00000584650.5:c.1813A>C
NM_001165962.1:c.2294A>C	NP_001159434.1:p.Asp765Ala
NM_018127.6:c.2414A>C	NP_060597.4:p.Asp805Ala
NM_173717.1:c.2411A>C	NP_776065.1:p.Asp804Ala
XM_024450850.1:c.2573A>C	XP_024306618.1:p.Asp858Ala
XM_024450851.1:c.2495A>C	XP_024306619.1:p.Asp832Ala
XM_024450852.1:c.2492A>C	XP_024306620.1:p.Asp831Ala
XM_024450853.1:c.2489A>C	XP_024306621.1:p.Asp830Ala
XM_024450854.1:c.2453A>C	XP_024306622.1:p.Asp818Ala
XM_024450855.1:c.2372A>C	XP_024306623.1:p.Asp791Ala
XM_024450856.1:c.2291A>C	XP_024306624.1:p.Asp764Ala
XM_024450857.1:c.2291A>C	XP_024306625.1:p.Asp764Ala
XM_024450858.1:c.2210A>C	XP_024306626.1:p.Asp737Ala
XM_024450859.1:c.2207A>C	XP_024306627.1:p.Asp736Ala
XM_024450860.1:c.2132A>C	XP_024306628.1:p.Asp711Ala
XM_024450861.1:c.2132A>C	XP_024306629.1:p.Asp711Ala
XM_024450862.1:c.2129A>C	XP_024306630.1:p.Asp710Ala
NM_018127.7:c.2414A>C MANE Select	NP_060597.4:p.Asp805Ala
NM_001165962.2:c.2294A>C	NP_001159434.1:p.Asp765Ala
NM_173717.2:c.2411A>C	NP_776065.1:p.Asp804Ala