Canonical Allele Identifier: CA2466520914

Linked Data

dbSNP Id: rs2064971716

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906781dup , CM000685.2:g.153906781dup GRCh38
NC_000023.10:g.153172235dup , CM000685.1:g.153172235dup GRCh37
NC_000023.9:g.152825429dup NCBI36
NG_008687.1:g.6808dup
NG_009645.3:g.7444dup
NG_013220.1:g.24481dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*53dup (AVPR2) MANE Select ENSP00000496396.1:n.*53dup
ENST00000434679.6:c.*535dup (AVPR2) ENSP00000393397.1:n.*535dup
ENST00000642393.1:c.97+2290dup
ENST00000646191.1:c.97+2290dup
ENST00000646375.1:c.*53dup (AVPR2) ENSP00000496396.1:n.*53dup
ENST00000337474.5:c.*53dup (AVPR2) ENSP00000338072.5:n.*53dup
ENST00000358927.6:c.*53dup (AVPR2) ENSP00000351805.2:n.*53dup
ENST00000430697.1:c.1081dup (AVPR2) ENSP00000393513.1:p.Leu361ProfsTer?
ENST00000434679.5:c.*535dup (AVPR2) ENSP00000393397.1:n.*535dup
ENST00000464967.5:n.154+2290dup (L1CAM)
NM_000054.4:c.*53dup (AVPR2) NP_000045.1:n.*53dup
NM_001146151.1:c.*345dup (AVPR2) NP_001139623.1:n.*345dup
NR_027419.1:n.1216dup (AVPR2)
XM_006724828.2:c.*53dup (AVPR2) XP_006724891.1:n.*53dup
NM_000054.5:c.*53dup (AVPR2) NP_000045.1:n.*53dup
NM_001146151.2:c.*345dup (AVPR2) NP_001139623.1:n.*345dup
XM_006724828.3:c.*53dup (AVPR2) XP_006724891.1:n.*53dup
NM_000054.6:c.*53dup (AVPR2) NP_000045.1:n.*53dup
NM_001146151.3:c.*345dup (AVPR2) NP_001139623.1:n.*345dup
NR_027419.2:n.1122dup (AVPR2)
NM_000054.7:c.*53dup (AVPR2) MANE Select NP_000045.1:n.*53dup