Canonical Allele Identifier: CA2651674362
Gene: AVP HGNC NCBI

Linked Data

gnomAD v4: 20-3082746-T-TGGCGCG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082754_3082759dup , CM000682.2:g.3082754_3082759dup GRCh38
NC_000020.10:g.3063400_3063405dup , CM000682.1:g.3063400_3063405dup GRCh37
NC_000020.9:g.3011400_3011405dup NCBI36
NG_008663.1:g.6973_6978dup , LRG_715:g.6973_6978dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.373_378dup MANE Select ENSP00000369647.3:p.Ala126_Ser127insArgAla
NM_000490.4:c.373_378dup , LRG_715t1:c.373_378dup NP_000481.2:p.Ala126_Ser127insArgAla
XM_011529267.1:c.373_378dup XP_011527569.1:p.Ala126_Ser127insArgAla
XM_011529267.2:c.373_378dup XP_011527569.1:p.Ala126_Ser127insArgAla
NM_000490.5:c.373_378dup MANE Select NP_000481.2:p.Ala126_Ser127insArgAla
Search 100 bp 5'
Search 100 bp 3'