Canonical Allele Identifier: CA398222202

Gene: ELAC2

Linked Data

• gnomAD v4: 17-12992921-G-T
• MyVariant Identifiers: chr17:g.12896238G>T (hg19) ; chr17:g.12992921G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992921G>T , CM000679.2:g.12992921G>T	GRCh38
NC_000017.10:g.12896238G>T , CM000679.1:g.12896238G>T	GRCh37
NC_000017.9:g.12836963G>T	NCBI36
NG_015808.1:g.30144C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2378C>A MANE Select	ENSP00000337445.4:p.Ala793Asp
ENST00000338034.8:c.2378C>A	ENSP00000337445.4:p.Ala793Asp
ENST00000395962.6:c.2321C>A	ENSP00000379291.1:p.Ala774Asp
ENST00000426905.7:c.2258C>A	ENSP00000405223.3:p.Ala753Asp
ENST00000465825.5:n.2265C>A
ENST00000480891.5:n.2207C>A
ENST00000484122.5:n.3208C>A
ENST00000487229.6:n.1924C>A
ENST00000584650.5:c.1777C>A
NM_001165962.1:c.2258C>A	NP_001159434.1:p.Ala753Asp
NM_018127.6:c.2378C>A	NP_060597.4:p.Ala793Asp
NM_173717.1:c.2375C>A	NP_776065.1:p.Ala792Asp
XM_024450850.1:c.2537C>A	XP_024306618.1:p.Ala846Asp
XM_024450851.1:c.2459C>A	XP_024306619.1:p.Ala820Asp
XM_024450852.1:c.2456C>A	XP_024306620.1:p.Ala819Asp
XM_024450853.1:c.2453C>A	XP_024306621.1:p.Ala818Asp
XM_024450854.1:c.2417C>A	XP_024306622.1:p.Ala806Asp
XM_024450855.1:c.2336C>A	XP_024306623.1:p.Ala779Asp
XM_024450856.1:c.2255C>A	XP_024306624.1:p.Ala752Asp
XM_024450857.1:c.2255C>A	XP_024306625.1:p.Ala752Asp
XM_024450858.1:c.2174C>A	XP_024306626.1:p.Ala725Asp
XM_024450859.1:c.2171C>A	XP_024306627.1:p.Ala724Asp
XM_024450860.1:c.2096C>A	XP_024306628.1:p.Ala699Asp
XM_024450861.1:c.2096C>A	XP_024306629.1:p.Ala699Asp
XM_024450862.1:c.2093C>A	XP_024306630.1:p.Ala698Asp
NM_018127.7:c.2378C>A MANE Select	NP_060597.4:p.Ala793Asp
NM_001165962.2:c.2258C>A	NP_001159434.1:p.Ala753Asp
NM_173717.2:c.2375C>A	NP_776065.1:p.Ala792Asp