Canonical Allele Identifier: CA1857216889
Gene: VPS13A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77360664T= , CM000671.2:g.77360664T= GRCh38
NC_000009.11:g.79975580T= , CM000671.1:g.79975580T= GRCh37
NC_000009.10:g.79165400T= NCBI36
NG_008931.1:g.188220T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360280.8:c.8211+23T= MANE Select ENSP00000353422.3:n.8211+23T=
ENST00000643348.1:c.8211+23T= ENSP00000493592.1:n.8211+23T=
ENST00000645632.1:c.8211+23T= ENSP00000496361.1:n.8211+23T=
ENST00000357409.9:c.8211+23T= ENSP00000349985.5:n.8211+23T=
ENST00000360280.7:c.8211+23T= ENSP00000353422.3:n.8211+23T=
ENST00000376634.8:c.8211+23T= ENSP00000365821.4:n.8211+23T=
ENST00000376636.7:c.8094+23T= ENSP00000365823.3:n.8094+23T=
NM_001018037.1:c.8094+23T= NP_001018047.1:n.8094+23T=
NM_001018038.2:c.8211+23T= NP_001018048.1:n.8211+23T=
NM_015186.3:c.8211+23T= NP_056001.1:n.8211+23T=
NM_033305.2:c.8211+23T= NP_150648.2:n.8211+23T=
XR_242579.2:n.8563+23T=
XR_242580.3:n.8563+23T=
XR_929740.1:n.8563+23T=
XR_001746259.1:n.8563+23T=
XR_001746260.1:n.8563+23T=
NM_033305.3:c.8211+23T= MANE Select NP_150648.2:n.8211+23T=
NM_001018037.2:c.8094+23T= NP_001018047.1:n.8094+23T=
NM_001018038.3:c.8211+23T= NP_001018048.1:n.8211+23T=
NM_015186.4:c.8211+23T= NP_056001.1:n.8211+23T=