Canonical Allele Identifier: CA2285205691

Gene: AFG3L2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12351335G= , CM000680.2:g.12351335G=	GRCh38
NC_000018.9:g.12351334G= , CM000680.1:g.12351334G=	GRCh37
NC_000018.8:g.12341334G=	NCBI36
NG_023361.1:g.30942C= , LRG_666:g.30942C=

Transcript Alleles

HGVS	Amino-acid Change
NM_006796.3:c.1397C= MANE Select	NP_006787.2:p.Pro466=
ENST00000269143.8:c.1397C= MANE Select	ENSP00000269143.2:p.Pro466=
NM_006796.2:c.1397C= , LRG_666t1:c.1397C=	NP_006787.2:p.Pro466=
ENST00000269143.7:c.1397C=	ENSP00000269143.2:p.Pro466=
ENST00000687337.1:c.*993C=	ENSP00000508998.1:n.*993C=
ENST00000688199.1:c.1259C=	ENSP00000510237.1:p.Pro420=
ENST00000691179.1:c.1322C=	ENSP00000509010.1:p.Pro441=
ENST00000691970.1:c.*774C=	ENSP00000508440.1:n.*774C=
ENST00000692497.1:c.1397C=	ENSP00000509870.1:p.Pro466=
ENST00000692988.1:n.1215C=
XM_011525601.1:c.1397C=	XP_011523903.1:p.Pro466=
XM_011525601.3:c.1397C=	XP_011523903.1:p.Pro466=