Canonical Allele Identifier: CA398222168

Gene: ELAC2

Linked Data

• MyVariant Identifiers: chr17:g.12896218C>A (hg19) ; chr17:g.12992901C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12992901C>A , CM000679.2:g.12992901C>A	GRCh38
NC_000017.10:g.12896218C>A , CM000679.1:g.12896218C>A	GRCh37
NC_000017.9:g.12836943C>A	NCBI36
NG_015808.1:g.30164G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338034.9:c.2398G>T MANE Select	ENSP00000337445.4:p.Ala800Ser
ENST00000338034.8:c.2398G>T	ENSP00000337445.4:p.Ala800Ser
ENST00000395962.6:c.2341G>T	ENSP00000379291.1:p.Ala781Ser
ENST00000426905.7:c.2278G>T	ENSP00000405223.3:p.Ala760Ser
ENST00000465825.5:n.2285G>T
ENST00000480891.5:n.2227G>T
ENST00000484122.5:n.3228G>T
ENST00000487229.6:n.1944G>T
ENST00000584650.5:c.1797G>T
NM_001165962.1:c.2278G>T	NP_001159434.1:p.Ala760Ser
NM_018127.6:c.2398G>T	NP_060597.4:p.Ala800Ser
NM_173717.1:c.2395G>T	NP_776065.1:p.Ala799Ser
XM_024450850.1:c.2557G>T	XP_024306618.1:p.Ala853Ser
XM_024450851.1:c.2479G>T	XP_024306619.1:p.Ala827Ser
XM_024450852.1:c.2476G>T	XP_024306620.1:p.Ala826Ser
XM_024450853.1:c.2473G>T	XP_024306621.1:p.Ala825Ser
XM_024450854.1:c.2437G>T	XP_024306622.1:p.Ala813Ser
XM_024450855.1:c.2356G>T	XP_024306623.1:p.Ala786Ser
XM_024450856.1:c.2275G>T	XP_024306624.1:p.Ala759Ser
XM_024450857.1:c.2275G>T	XP_024306625.1:p.Ala759Ser
XM_024450858.1:c.2194G>T	XP_024306626.1:p.Ala732Ser
XM_024450859.1:c.2191G>T	XP_024306627.1:p.Ala731Ser
XM_024450860.1:c.2116G>T	XP_024306628.1:p.Ala706Ser
XM_024450861.1:c.2116G>T	XP_024306629.1:p.Ala706Ser
XM_024450862.1:c.2113G>T	XP_024306630.1:p.Ala705Ser
NM_018127.7:c.2398G>T MANE Select	NP_060597.4:p.Ala800Ser
NM_001165962.2:c.2278G>T	NP_001159434.1:p.Ala760Ser
NM_173717.2:c.2395G>T	NP_776065.1:p.Ala799Ser