Canonical Allele Identifier: CA401943644

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337362T>A (hg19) ; chr18:g.12337363T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337363T>A , CM000680.2:g.12337363T>A	GRCh38
NC_000018.9:g.12337362T>A , CM000680.1:g.12337362T>A	GRCh37
NC_000018.8:g.12327362T>A	NCBI36
NG_023361.1:g.44914A>T , LRG_666:g.44914A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1749A>T (AFG3L2)	ENSP00000508998.1:n.*1749A>T
ENST00000687477.1:n.689A>T (AFG3L2)
ENST00000688199.1:c.2015A>T (AFG3L2)	ENSP00000510237.1:p.Glu672Val
ENST00000691179.1:c.2078A>T (AFG3L2)	ENSP00000509010.1:p.Glu693Val
ENST00000691970.1:c.*1530A>T (AFG3L2)	ENSP00000508440.1:n.*1530A>T
ENST00000692497.1:c.*583A>T (AFG3L2)	ENSP00000509870.1:n.*583A>T
ENST00000692988.1:n.1971A>T (AFG3L2)
ENST00000269143.8:c.2153A>T (AFG3L2) MANE Select	ENSP00000269143.2:p.Glu718Val
ENST00000269143.7:c.2153A>T (AFG3L2)	ENSP00000269143.2:p.Glu718Val
ENST00000586691.1:c.88-6686T>A (TUBB6)
NM_006796.2:c.2153A>T , LRG_666t1:c.2153A>T (AFG3L2)	NP_006787.2:p.Glu718Val
XM_011525601.1:c.1952A>T (AFG3L2)	XP_011523903.1:p.Glu651Val
XM_011525601.3:c.1952A>T (AFG3L2)	XP_011523903.1:p.Glu651Val
XR_002958227.1:n.451+461T>A
NM_006796.3:c.2153A>T (AFG3L2) MANE Select	NP_006787.2:p.Glu718Val