Canonical Allele Identifier: CA498009598

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896216T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992899T>A , CM000679.2:g.12992899T>A	GRCh38
NC_000017.10:g.12896216T>A , CM000679.1:g.12896216T>A	GRCh37
NC_000017.9:g.12836941T>A	NCBI36
NG_015808.1:g.30166A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2400A>T MANE Select	ENSP00000337445.4:p.Ala800=
ENST00000338034.8:c.2400A>T	ENSP00000337445.4:p.Ala800=
ENST00000395962.6:c.2343A>T	ENSP00000379291.1:p.Ala781=
ENST00000426905.7:c.2280A>T	ENSP00000405223.3:p.Ala760=
ENST00000465825.5:n.2287A>T
ENST00000480891.5:n.2229A>T
ENST00000484122.5:n.3230A>T
ENST00000487229.6:n.1946A>T
ENST00000584650.5:c.1799A>T
NM_001165962.1:c.2280A>T	NP_001159434.1:p.Ala760=
NM_018127.6:c.2400A>T	NP_060597.4:p.Ala800=
NM_173717.1:c.2397A>T	NP_776065.1:p.Ala799=
XM_024450850.1:c.2559A>T	XP_024306618.1:p.Ala853=
XM_024450851.1:c.2481A>T	XP_024306619.1:p.Ala827=
XM_024450852.1:c.2478A>T	XP_024306620.1:p.Ala826=
XM_024450853.1:c.2475A>T	XP_024306621.1:p.Ala825=
XM_024450854.1:c.2439A>T	XP_024306622.1:p.Ala813=
XM_024450855.1:c.2358A>T	XP_024306623.1:p.Ala786=
XM_024450856.1:c.2277A>T	XP_024306624.1:p.Ala759=
XM_024450857.1:c.2277A>T	XP_024306625.1:p.Ala759=
XM_024450858.1:c.2196A>T	XP_024306626.1:p.Ala732=
XM_024450859.1:c.2193A>T	XP_024306627.1:p.Ala731=
XM_024450860.1:c.2118A>T	XP_024306628.1:p.Ala706=
XM_024450861.1:c.2118A>T	XP_024306629.1:p.Ala706=
XM_024450862.1:c.2115A>T	XP_024306630.1:p.Ala705=
NM_018127.7:c.2400A>T MANE Select	NP_060597.4:p.Ala800=
NM_001165962.2:c.2280A>T	NP_001159434.1:p.Ala760=
NM_173717.2:c.2397A>T	NP_776065.1:p.Ala799=