Canonical Allele Identifier: CA401951721

Gene: AFG3L2

Linked Data

• MyVariant Identifiers: chr18:g.12351096G>C (hg19) ; chr18:g.12351097G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12351097G>C , CM000680.2:g.12351097G>C	GRCh38
NC_000018.9:g.12351096G>C , CM000680.1:g.12351096G>C	GRCh37
NC_000018.8:g.12341096G>C	NCBI36
NG_023361.1:g.31180C>G , LRG_666:g.31180C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*1136C>G	ENSP00000508998.1:n.*1136C>G
ENST00000688199.1:c.1402C>G	ENSP00000510237.1:p.Pro468Ala
ENST00000691179.1:c.1465C>G	ENSP00000509010.1:p.Pro489Ala
ENST00000691970.1:c.*917C>G	ENSP00000508440.1:n.*917C>G
ENST00000692497.1:c.1540C>G	ENSP00000509870.1:p.Pro514Ala
ENST00000692988.1:n.1358C>G
ENST00000269143.8:c.1540C>G MANE Select	ENSP00000269143.2:p.Pro514Ala
ENST00000269143.7:c.1540C>G	ENSP00000269143.2:p.Pro514Ala
NM_006796.2:c.1540C>G , LRG_666t1:c.1540C>G	NP_006787.2:p.Pro514Ala
XM_011525601.1:c.1540C>G	XP_011523903.1:p.Pro514Ala
XM_011525601.3:c.1540C>G	XP_011523903.1:p.Pro514Ala
NM_006796.3:c.1540C>G MANE Select	NP_006787.2:p.Pro514Ala