Canonical Allele Identifier: CA9924145

Gene: VAPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58389522G>A , CM000682.2:g.58389522G>A	GRCh38
NC_000020.10:g.56964578G>A , CM000682.1:g.56964578G>A	GRCh37
NC_000020.9:g.56397984G>A	NCBI36
NG_008073.2:g.5334G>A , LRG_656:g.5334G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004738.5:c.58+5G>A MANE Select	NP_004729.1:n.58+5G>A
ENST00000475243.6:c.58+5G>A MANE Select	ENSP00000417175.1:n.58+5G>A
NM_001195677.1:c.58+5G>A	NP_001182606.1:n.58+5G>A
NM_001195677.2:c.58+5G>A	NP_001182606.1:n.58+5G>A
NM_004738.4:c.58+5G>A , LRG_656t1:c.58+5G>A	NP_004729.1:n.58+5G>A
NR_036633.1:n.399+5G>A
NR_036633.2:n.289+5G>A
ENST00000265619.6:n.143+5G>A
ENST00000395802.7:c.58+5G>A	ENSP00000379147.3:n.58+5G>A
ENST00000475243.5:c.58+5G>A	ENSP00000417175.1:n.58+5G>A
ENST00000520497.1:c.58+5G>A	ENSP00000430426.1:n.58+5G>A
XR_001754433.2:n.307+5G>A