Canonical Allele Identifier: CA511065944

Gene: VAPB

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.58418251C>T , CM000682.2:g.58418251C>T	GRCh38
NC_000020.10:g.56993307C>T , CM000682.1:g.56993307C>T	GRCh37
NC_000020.9:g.56426713C>T	NCBI36
NG_008073.2:g.34063C>T , LRG_656:g.34063C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004738.5:c.99C>T MANE Select	NP_004729.1:p.Gly33=
ENST00000475243.6:c.99C>T MANE Select	ENSP00000417175.1:p.Gly33=
NM_001195677.1:c.99C>T	NP_001182606.1:p.Gly33=
NM_001195677.2:c.99C>T	NP_001182606.1:p.Gly33=
NM_004738.4:c.99C>T , LRG_656t1:c.99C>T	NP_004729.1:p.Gly33=
NR_036633.1:n.440C>T
NR_036633.2:n.330C>T
ENST00000265619.6:n.397C>T
ENST00000395802.7:c.99C>T	ENSP00000379147.3:p.Gly33=
ENST00000475243.5:c.99C>T	ENSP00000417175.1:p.Gly33=
ENST00000520497.1:c.99C>T	ENSP00000430426.1:p.Gly33=
XR_001754433.2:n.348C>T