Canonical Allele Identifier: CA321184580
Gene: ATP6V1E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17600825T>C , CM000684.2:g.17600825T>C GRCh38
NC_000022.10:g.18083591T>C , CM000684.1:g.18083591T>C GRCh37
NC_000022.9:g.16463591T>C NCBI36
NG_009214.1:g.32998A>G
NG_009214.2:g.32998A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001696.4:c.366+267A>G MANE Select NP_001687.1:n.366+267A>G
ENST00000253413.10:c.366+267A>G MANE Select ENSP00000253413.5:n.366+267A>G
NM_001039366.1:c.300+267A>G NP_001034455.1:n.300+267A>G
NM_001039367.1:c.277-730A>G NP_001034456.1:n.277-730A>G
NM_001696.3:c.366+267A>G NP_001687.1:n.366+267A>G
ENST00000253413.9:c.366+267A>G ENSP00000253413.5:n.366+267A>G
ENST00000399796.6:c.277-730A>G ENSP00000382694.2:n.277-730A>G
ENST00000399798.6:c.300+267A>G ENSP00000382696.2:n.300+267A>G
ENST00000413576.1:c.369+267A>G ENSP00000398932.1:n.369+267A>G
ENST00000481365.5:n.335+267A>G
ENST00000484653.5:n.602A>G