Canonical Allele Identifier: CA511065597

Gene: VAPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58418215C>G , CM000682.2:g.58418215C>G	GRCh38
NC_000020.10:g.56993271C>G , CM000682.1:g.56993271C>G	GRCh37
NC_000020.9:g.56426677C>G	NCBI36
NG_008073.2:g.34027C>G , LRG_656:g.34027C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004738.5:c.63C>G MANE Select	NP_004729.1:p.Pro21=
ENST00000475243.6:c.63C>G MANE Select	ENSP00000417175.1:p.Pro21=
NM_001195677.1:c.63C>G	NP_001182606.1:p.Pro21=
NM_001195677.2:c.63C>G	NP_001182606.1:p.Pro21=
NM_004738.4:c.63C>G , LRG_656t1:c.63C>G	NP_004729.1:p.Pro21=
NR_036633.1:n.404C>G
NR_036633.2:n.294C>G
ENST00000265619.6:n.361C>G
ENST00000395802.7:c.63C>G	ENSP00000379147.3:p.Pro21=
ENST00000475243.5:c.63C>G	ENSP00000417175.1:p.Pro21=
ENST00000520497.1:c.63C>G	ENSP00000430426.1:p.Pro21=
XR_001754433.2:n.312C>G