Canonical Allele Identifier: CA415112383

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906748C>G , CM000685.2:g.153906748C>G GRCh38
NC_000023.10:g.153172202C>G , CM000685.1:g.153172202C>G GRCh37
NC_000023.9:g.152825396C>G NCBI36
NG_008687.1:g.6775C>G
NG_009645.3:g.7476G>C
NG_013220.1:g.24513G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*20C>G (AVPR2) MANE Select ENSP00000496396.1:n.*20C>G
ENST00000434679.6:c.*502C>G (AVPR2) ENSP00000393397.1:n.*502C>G
ENST00000642393.1:c.97+2322G>C
ENST00000646191.1:c.97+2322G>C
ENST00000646375.1:c.*20C>G (AVPR2) ENSP00000496396.1:n.*20C>G
ENST00000337474.5:c.*20C>G (AVPR2) ENSP00000338072.5:n.*20C>G
ENST00000358927.6:c.*20C>G (AVPR2) ENSP00000351805.2:n.*20C>G
ENST00000370049.1:c.*312C>G (AVPR2) ENSP00000359066.1:n.*312C>G
ENST00000430697.1:c.1048C>G (AVPR2) ENSP00000393513.1:p.Pro350Ala
ENST00000434679.5:c.*502C>G (AVPR2) ENSP00000393397.1:n.*502C>G
ENST00000464967.5:n.154+2322G>C (L1CAM)
NM_000054.4:c.*20C>G (AVPR2) NP_000045.1:n.*20C>G
NM_001146151.1:c.*312C>G (AVPR2) NP_001139623.1:n.*312C>G
NR_027419.1:n.1183C>G (AVPR2)
XM_006724828.2:c.*20C>G (AVPR2) XP_006724891.1:n.*20C>G
NM_000054.5:c.*20C>G (AVPR2) NP_000045.1:n.*20C>G
NM_001146151.2:c.*312C>G (AVPR2) NP_001139623.1:n.*312C>G
XM_006724828.3:c.*20C>G (AVPR2) XP_006724891.1:n.*20C>G
NM_000054.6:c.*20C>G (AVPR2) NP_000045.1:n.*20C>G
NM_001146151.3:c.*312C>G (AVPR2) NP_001139623.1:n.*312C>G
NR_027419.2:n.1089C>G (AVPR2)
NM_000054.7:c.*20C>G (AVPR2) MANE Select NP_000045.1:n.*20C>G