Canonical Allele Identifier: CA636212155

Gene: VAPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58389527A>G , CM000682.2:g.58389527A>G	GRCh38
NC_000020.10:g.56964583A>G , CM000682.1:g.56964583A>G	GRCh37
NC_000020.9:g.56397989A>G	NCBI36
NG_008073.2:g.5339A>G , LRG_656:g.5339A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004738.5:c.58+10A>G MANE Select	NP_004729.1:n.58+10A>G
ENST00000475243.6:c.58+10A>G MANE Select	ENSP00000417175.1:n.58+10A>G
NM_001195677.1:c.58+10A>G	NP_001182606.1:n.58+10A>G
NM_001195677.2:c.58+10A>G	NP_001182606.1:n.58+10A>G
NM_004738.4:c.58+10A>G , LRG_656t1:c.58+10A>G	NP_004729.1:n.58+10A>G
NR_036633.1:n.399+10A>G
NR_036633.2:n.289+10A>G
ENST00000265619.6:n.143+10A>G
ENST00000395802.7:c.58+10A>G	ENSP00000379147.3:n.58+10A>G
ENST00000475243.5:c.58+10A>G	ENSP00000417175.1:n.58+10A>G
ENST00000520497.1:c.58+10A>G	ENSP00000430426.1:n.58+10A>G
XR_001754433.2:n.307+10A>G