Canonical Allele Identifier: CA2346405159
Gene: AVP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082662_3082664delinsGCT , CM000682.2:g.3082662_3082664delinsGCT GRCh38
NC_000020.10:g.3063308_3063310delinsGCT , CM000682.1:g.3063308_3063310delinsGCT GRCh37
NC_000020.9:g.3011308_3011310delinsGCT NCBI36
NG_008663.1:g.7061_7063delinsAGC , LRG_715:g.7061_7063delinsAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.461_463delinsAGC MANE Select ENSP00000369647.3:p.Glu154=
NM_000490.4:c.461_463delinsAGC , LRG_715t1:c.461_463delinsAGC NP_000481.2:p.Glu154=
XM_011529267.1:c.461_463delinsAGC XP_011527569.1:p.Glu154=
XM_011529267.2:c.461_463delinsAGC XP_011527569.1:p.Glu154=
NM_000490.5:c.461_463delinsAGC MANE Select NP_000481.2:p.Glu154=