Canonical Allele Identifier: CA2466520926

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906815C= , CM000685.2:g.153906815C= GRCh38
NC_000023.10:g.153172269C= , CM000685.1:g.153172269C= GRCh37
NC_000023.9:g.152825463C= NCBI36
NG_008687.1:g.6842C=
NG_009645.3:g.7409G=
NG_013220.1:g.24446G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*87C= (AVPR2) MANE Select ENSP00000496396.1:n.*87C=
ENST00000434679.6:c.*569C= (AVPR2) ENSP00000393397.1:n.*569C=
ENST00000642393.1:c.97+2255G=
ENST00000646191.1:c.97+2255G=
ENST00000646375.1:c.*87C= (AVPR2) ENSP00000496396.1:n.*87C=
ENST00000337474.5:c.*87C= (AVPR2) ENSP00000338072.5:n.*87C=
ENST00000358927.6:c.*87C= (AVPR2) ENSP00000351805.2:n.*87C=
ENST00000430697.1:c.1115C= (AVPR2) ENSP00000393513.1:p.Thr372=
ENST00000434679.5:c.*569C= (AVPR2) ENSP00000393397.1:n.*569C=
ENST00000464967.5:n.154+2255G= (L1CAM)
NM_000054.4:c.*87C= (AVPR2) NP_000045.1:n.*87C=
NM_001146151.1:c.*379C= (AVPR2) NP_001139623.1:n.*379C=
NR_027419.1:n.1250C= (AVPR2)
XM_006724828.2:c.*87C= (AVPR2) XP_006724891.1:n.*87C=
NM_000054.5:c.*87C= (AVPR2) NP_000045.1:n.*87C=
NM_001146151.2:c.*379C= (AVPR2) NP_001139623.1:n.*379C=
XM_006724828.3:c.*87C= (AVPR2) XP_006724891.1:n.*87C=
NM_000054.6:c.*87C= (AVPR2) NP_000045.1:n.*87C=
NM_001146151.3:c.*379C= (AVPR2) NP_001139623.1:n.*379C=
NR_027419.2:n.1156C= (AVPR2)
NM_000054.7:c.*87C= (AVPR2) MANE Select NP_000045.1:n.*87C=