Canonical Allele Identifier: CA2651674500
Gene: AVP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082877_3082883del , CM000682.2:g.3082877_3082883del GRCh38
NC_000020.10:g.3063523_3063529del , CM000682.1:g.3063523_3063529del GRCh37
NC_000020.9:g.3011523_3011529del NCBI36
NG_008663.1:g.6842_6848del , LRG_715:g.6842_6848del

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.323-81_323-75del MANE Select ENSP00000369647.3:n.323-81_323-75del
NM_000490.4:c.323-81_323-75del , LRG_715t1:c.323-81_323-75del NP_000481.2:n.323-81_323-75del
XM_011529267.1:c.323-81_323-75del XP_011527569.1:n.323-81_323-75del
XM_011529267.2:c.323-81_323-75del XP_011527569.1:n.323-81_323-75del
NM_000490.5:c.323-81_323-75del MANE Select NP_000481.2:n.323-81_323-75del