Canonical Allele Identifier: CA1857190157
Gene: VPS13A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.77302901A= , CM000671.2:g.77302901A= GRCh38
NC_000009.11:g.79917817A= , CM000671.1:g.79917817A= GRCh37
NC_000009.10:g.79107637A= NCBI36
NG_008931.1:g.130457A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360280.8:c.3813-14A= MANE Select ENSP00000353422.3:n.3813-14A=
ENST00000643348.1:c.3813-14A= ENSP00000493592.1:n.3813-14A=
ENST00000645632.1:c.3813-14A= ENSP00000496361.1:n.3813-14A=
ENST00000357409.9:c.3813-14A= ENSP00000349985.5:n.3813-14A=
ENST00000360280.7:c.3813-14A= ENSP00000353422.3:n.3813-14A=
ENST00000376634.8:c.3813-14A= ENSP00000365821.4:n.3813-14A=
ENST00000376636.7:c.3696-14A= ENSP00000365823.3:n.3696-14A=
ENST00000423463.6:n.1103-14A=
ENST00000493341.1:c.321-14A= ENSP00000437478.1:n.321-14A=
NM_001018037.1:c.3696-14A= NP_001018047.1:n.3696-14A=
NM_001018038.2:c.3813-14A= NP_001018048.1:n.3813-14A=
NM_015186.3:c.3813-14A= NP_056001.1:n.3813-14A=
NM_033305.2:c.3813-14A= NP_150648.2:n.3813-14A=
XR_242579.2:n.4165-14A=
XR_242580.3:n.4165-14A=
XR_929740.1:n.4165-14A=
XR_001746259.1:n.4165-14A=
XR_001746260.1:n.4165-14A=
NM_033305.3:c.3813-14A= MANE Select NP_150648.2:n.3813-14A=
NM_001018037.2:c.3696-14A= NP_001018047.1:n.3696-14A=
NM_001018038.3:c.3813-14A= NP_001018048.1:n.3813-14A=
NM_015186.4:c.3813-14A= NP_056001.1:n.3813-14A=