Canonical Allele Identifier: CA2466520915

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906780C= , CM000685.2:g.153906780C= GRCh38
NC_000023.10:g.153172234C= , CM000685.1:g.153172234C= GRCh37
NC_000023.9:g.152825428C= NCBI36
NG_008687.1:g.6807C=
NG_009645.3:g.7444G=
NG_013220.1:g.24481G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*52C= (AVPR2) MANE Select ENSP00000496396.1:n.*52C=
ENST00000434679.6:c.*534C= (AVPR2) ENSP00000393397.1:n.*534C=
ENST00000642393.1:c.97+2290G=
ENST00000646191.1:c.97+2290G=
ENST00000646375.1:c.*52C= (AVPR2) ENSP00000496396.1:n.*52C=
ENST00000337474.5:c.*52C= (AVPR2) ENSP00000338072.5:n.*52C=
ENST00000358927.6:c.*52C= (AVPR2) ENSP00000351805.2:n.*52C=
ENST00000370049.1:c.*344C= (AVPR2) ENSP00000359066.1:n.*344C=
ENST00000430697.1:c.1080C= (AVPR2) ENSP00000393513.1:p.Phe360=
ENST00000434679.5:c.*534C= (AVPR2) ENSP00000393397.1:n.*534C=
ENST00000464967.5:n.154+2290G= (L1CAM)
NM_000054.4:c.*52C= (AVPR2) NP_000045.1:n.*52C=
NM_001146151.1:c.*344C= (AVPR2) NP_001139623.1:n.*344C=
NR_027419.1:n.1215C= (AVPR2)
XM_006724828.2:c.*52C= (AVPR2) XP_006724891.1:n.*52C=
NM_000054.5:c.*52C= (AVPR2) NP_000045.1:n.*52C=
NM_001146151.2:c.*344C= (AVPR2) NP_001139623.1:n.*344C=
XM_006724828.3:c.*52C= (AVPR2) XP_006724891.1:n.*52C=
NM_000054.6:c.*52C= (AVPR2) NP_000045.1:n.*52C=
NM_001146151.3:c.*344C= (AVPR2) NP_001139623.1:n.*344C=
NR_027419.2:n.1121C= (AVPR2)
NM_000054.7:c.*52C= (AVPR2) MANE Select NP_000045.1:n.*52C=