Canonical Allele Identifier: CA321184108
Community Standard Title: NM_001696.4(ATP6V1E1):c.435+9C>T
Gene: ATP6V1E1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.17600018G>A , CM000684.2:g.17600018G>A GRCh38
NC_000022.10:g.18082784G>A , CM000684.1:g.18082784G>A GRCh37
NC_000022.9:g.16462784G>A NCBI36
NG_009214.1:g.33805C>T
NG_009214.2:g.33805C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001696.4:c.435+9C>T MANE Select NP_001687.1:n.435+9C>T
ENST00000253413.10:c.435+9C>T MANE Select ENSP00000253413.5:n.435+9C>T
NM_001039366.1:c.369+9C>T NP_001034455.1:n.369+9C>T
NM_001039367.1:c.345+9C>T NP_001034456.1:n.345+9C>T
NM_001696.3:c.435+9C>T NP_001687.1:n.435+9C>T
ENST00000253413.9:c.435+9C>T ENSP00000253413.5:n.435+9C>T
ENST00000399796.6:c.345+9C>T ENSP00000382694.2:n.345+9C>T
ENST00000399798.6:c.369+9C>T ENSP00000382696.2:n.369+9C>T
ENST00000413576.1:c.438+9C>T ENSP00000398932.1:n.438+9C>T
ENST00000481365.5:n.404+9C>T