Canonical Allele Identifier: CA401953521

Gene: AFG3L2

Linked Data

• MyVariant Identifiers: chr18:g.12358736A>C (hg19) ; chr18:g.12358737A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12358737A>C , CM000680.2:g.12358737A>C	GRCh38
NC_000018.9:g.12358736A>C , CM000680.1:g.12358736A>C	GRCh37
NC_000018.8:g.12348736A>C	NCBI36
NG_023361.1:g.23540T>G , LRG_666:g.23540T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000687337.1:c.*555T>G	ENSP00000508998.1:n.*555T>G
ENST00000688199.1:c.959T>G	ENSP00000510237.1:p.Ile320Ser
ENST00000691179.1:c.884T>G	ENSP00000509010.1:p.Ile295Ser
ENST00000691970.1:c.*336T>G	ENSP00000508440.1:n.*336T>G
ENST00000692497.1:c.959T>G	ENSP00000509870.1:p.Ile320Ser
ENST00000692988.1:n.777T>G
ENST00000269143.8:c.959T>G MANE Select	ENSP00000269143.2:p.Ile320Ser
ENST00000269143.7:c.959T>G	ENSP00000269143.2:p.Ile320Ser
ENST00000590811.1:c.594T>G
NM_006796.2:c.959T>G , LRG_666t1:c.959T>G	NP_006787.2:p.Ile320Ser
XM_011525601.1:c.959T>G	XP_011523903.1:p.Ile320Ser
XM_011525601.3:c.959T>G	XP_011523903.1:p.Ile320Ser
NM_006796.3:c.959T>G MANE Select	NP_006787.2:p.Ile320Ser