Canonical Allele Identifier: CA5091890
Gene: VPS13A HGNC NCBI

Linked Data

ClinVar Variation Id: 367364
dbSNP Id: rs117320408
gnomAD v2: 9-79867181-G-A
gnomAD v3: 9-77252265-G-A
gnomAD v4: 9-77252265-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77252265G>A , CM000671.2:g.77252265G>A GRCh38
NC_000009.11:g.79867181G>A , CM000671.1:g.79867181G>A GRCh37
NC_000009.10:g.79057001G>A NCBI36
NG_008931.1:g.79821G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360280.8:c.2201G>A MANE Select ENSP00000353422.3:p.Ser734Asn
ENST00000643348.1:c.2201G>A ENSP00000493592.1:p.Ser734Asn
ENST00000645632.1:c.2201G>A ENSP00000496361.1:p.Ser734Asn
ENST00000357409.9:c.2201G>A ENSP00000349985.5:p.Ser734Asn
ENST00000360280.7:c.2201G>A ENSP00000353422.3:p.Ser734Asn
ENST00000376634.8:c.2201G>A ENSP00000365821.4:p.Ser734Asn
ENST00000376636.7:c.2201G>A ENSP00000365823.3:p.Ser734Asn
NM_001018037.1:c.2201G>A NP_001018047.1:p.Ser734Asn
NM_001018038.2:c.2201G>A NP_001018048.1:p.Ser734Asn
NM_015186.3:c.2201G>A NP_056001.1:p.Ser734Asn
NM_033305.2:c.2201G>A NP_150648.2:p.Ser734Asn
XR_242579.2:n.2553G>A
XR_242580.3:n.2553G>A
XR_929740.1:n.2553G>A
XR_001746259.1:n.2553G>A
XR_001746260.1:n.2553G>A
NM_033305.3:c.2201G>A MANE Select NP_150648.2:p.Ser734Asn
NM_001018037.2:c.2201G>A NP_001018047.1:p.Ser734Asn
NM_001018038.3:c.2201G>A NP_001018048.1:p.Ser734Asn
NM_015186.4:c.2201G>A NP_056001.1:p.Ser734Asn