Canonical Allele Identifier: CA401943972

Gene: AFG3L2 TUBB6

Linked Data

• MyVariant Identifiers: chr18:g.12337434G>A (hg19) ; chr18:g.12337435G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.12337435G>A , CM000680.2:g.12337435G>A	GRCh38
NC_000018.9:g.12337434G>A , CM000680.1:g.12337434G>A	GRCh37
NC_000018.8:g.12327434G>A	NCBI36
NG_023361.1:g.44842C>T , LRG_666:g.44842C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687337.1:c.*1677C>T (AFG3L2)	ENSP00000508998.1:n.*1677C>T
ENST00000687477.1:n.617C>T (AFG3L2)
ENST00000688199.1:c.1943C>T (AFG3L2)	ENSP00000510237.1:p.Ala648Val
ENST00000691179.1:c.2006C>T (AFG3L2)	ENSP00000509010.1:p.Ala669Val
ENST00000691970.1:c.*1458C>T (AFG3L2)	ENSP00000508440.1:n.*1458C>T
ENST00000692497.1:c.*511C>T (AFG3L2)	ENSP00000509870.1:n.*511C>T
ENST00000692988.1:n.1899C>T (AFG3L2)
ENST00000269143.8:c.2081C>T (AFG3L2) MANE Select	ENSP00000269143.2:p.Ala694Val
ENST00000269143.7:c.2081C>T (AFG3L2)	ENSP00000269143.2:p.Ala694Val
ENST00000586691.1:c.88-6614G>A (TUBB6)
NM_006796.2:c.2081C>T , LRG_666t1:c.2081C>T (AFG3L2)	NP_006787.2:p.Ala694Val
XM_011525601.1:c.1880C>T (AFG3L2)	XP_011523903.1:p.Ala627Val
XM_011525601.3:c.1880C>T (AFG3L2)	XP_011523903.1:p.Ala627Val
XR_002958227.1:n.451+533G>A
NM_006796.3:c.2081C>T (AFG3L2) MANE Select	NP_006787.2:p.Ala694Val