Canonical Allele Identifier: CA398222109

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896190T>G (hg19) ; chr17:g.12992873T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992873T>G , CM000679.2:g.12992873T>G	GRCh38
NC_000017.10:g.12896190T>G , CM000679.1:g.12896190T>G	GRCh37
NC_000017.9:g.12836915T>G	NCBI36
NG_015808.1:g.30192A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2426A>C MANE Select	ENSP00000337445.4:p.Gln809Pro
ENST00000338034.8:c.2426A>C	ENSP00000337445.4:p.Gln809Pro
ENST00000395962.6:c.2369A>C	ENSP00000379291.1:p.Gln790Pro
ENST00000426905.7:c.2306A>C	ENSP00000405223.3:p.Gln769Pro
ENST00000465825.5:n.2313A>C
ENST00000480891.5:n.2255A>C
ENST00000484122.5:n.3256A>C
ENST00000487229.6:n.1972A>C
ENST00000584650.5:c.1825A>C
NM_001165962.1:c.2306A>C	NP_001159434.1:p.Gln769Pro
NM_018127.6:c.2426A>C	NP_060597.4:p.Gln809Pro
NM_173717.1:c.2423A>C	NP_776065.1:p.Gln808Pro
XM_024450850.1:c.2585A>C	XP_024306618.1:p.Gln862Pro
XM_024450851.1:c.2507A>C	XP_024306619.1:p.Gln836Pro
XM_024450852.1:c.2504A>C	XP_024306620.1:p.Gln835Pro
XM_024450853.1:c.2501A>C	XP_024306621.1:p.Gln834Pro
XM_024450854.1:c.2465A>C	XP_024306622.1:p.Gln822Pro
XM_024450855.1:c.2384A>C	XP_024306623.1:p.Gln795Pro
XM_024450856.1:c.2303A>C	XP_024306624.1:p.Gln768Pro
XM_024450857.1:c.2303A>C	XP_024306625.1:p.Gln768Pro
XM_024450858.1:c.2222A>C	XP_024306626.1:p.Gln741Pro
XM_024450859.1:c.2219A>C	XP_024306627.1:p.Gln740Pro
XM_024450860.1:c.2144A>C	XP_024306628.1:p.Gln715Pro
XM_024450861.1:c.2144A>C	XP_024306629.1:p.Gln715Pro
XM_024450862.1:c.2141A>C	XP_024306630.1:p.Gln714Pro
NM_018127.7:c.2426A>C MANE Select	NP_060597.4:p.Gln809Pro
NM_001165962.2:c.2306A>C	NP_001159434.1:p.Gln769Pro
NM_173717.2:c.2423A>C	NP_776065.1:p.Gln808Pro