Canonical Allele Identifier: CA401951781

Gene: AFG3L2

Linked Data

• MyVariant Identifiers: chr18:g.12351112T>A (hg19) ; chr18:g.12351113T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12351113T>A , CM000680.2:g.12351113T>A	GRCh38
NC_000018.9:g.12351112T>A , CM000680.1:g.12351112T>A	GRCh37
NC_000018.8:g.12341112T>A	NCBI36
NG_023361.1:g.31164A>T , LRG_666:g.31164A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1120A>T	ENSP00000508998.1:n.*1120A>T
ENST00000688199.1:c.1386A>T	ENSP00000510237.1:p.Lys462Asn
ENST00000691179.1:c.1449A>T	ENSP00000509010.1:p.Lys483Asn
ENST00000691970.1:c.*901A>T	ENSP00000508440.1:n.*901A>T
ENST00000692497.1:c.1524A>T	ENSP00000509870.1:p.Lys508Asn
ENST00000692988.1:n.1342A>T
ENST00000269143.8:c.1524A>T MANE Select	ENSP00000269143.2:p.Lys508Asn
ENST00000269143.7:c.1524A>T	ENSP00000269143.2:p.Lys508Asn
NM_006796.2:c.1524A>T , LRG_666t1:c.1524A>T	NP_006787.2:p.Lys508Asn
XM_011525601.1:c.1524A>T	XP_011523903.1:p.Lys508Asn
XM_011525601.3:c.1524A>T	XP_011523903.1:p.Lys508Asn
NM_006796.3:c.1524A>T MANE Select	NP_006787.2:p.Lys508Asn