Canonical Allele Identifier: CA9924166

Gene: VAPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58418195_58418196del , CM000682.2:g.58418195_58418196del	GRCh38
NC_000020.10:g.56993251_56993252del , CM000682.1:g.56993251_56993252del	GRCh37
NC_000020.9:g.56426657_56426658del	NCBI36
NG_008073.2:g.34007_34008del , LRG_656:g.34007_34008del

Transcript Alleles

HGVS	Amino-acid Change
NM_004738.5:c.59-16_59-15del MANE Select	NP_004729.1:n.59-16_59-15del
ENST00000475243.6:c.59-16_59-15del MANE Select	ENSP00000417175.1:n.59-16_59-15del
NM_001195677.1:c.59-16_59-15del	NP_001182606.1:n.59-16_59-15del
NM_001195677.2:c.59-16_59-15del	NP_001182606.1:n.59-16_59-15del
NM_004738.4:c.59-16_59-15del , LRG_656t1:c.59-16_59-15del	NP_004729.1:n.59-16_59-15del
NR_036633.1:n.400-16_400-15del
NR_036633.2:n.290-16_290-15del
ENST00000265619.6:n.357-16_357-15del
ENST00000395802.7:c.59-16_59-15del	ENSP00000379147.3:n.59-16_59-15del
ENST00000475243.5:c.59-16_59-15del	ENSP00000417175.1:n.59-16_59-15del
ENST00000520497.1:c.59-16_59-15del	ENSP00000430426.1:n.59-16_59-15del
XR_001754433.2:n.308-16_308-15del