Canonical Allele Identifier: CA415112593

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906776C>G , CM000685.2:g.153906776C>G GRCh38
NC_000023.10:g.153172230C>G , CM000685.1:g.153172230C>G GRCh37
NC_000023.9:g.152825424C>G NCBI36
NG_008687.1:g.6803C>G
NG_009645.3:g.7448G>C
NG_013220.1:g.24485G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*48C>G (AVPR2) MANE Select ENSP00000496396.1:n.*48C>G
ENST00000434679.6:c.*530C>G (AVPR2) ENSP00000393397.1:n.*530C>G
ENST00000642393.1:c.97+2294G>C
ENST00000646191.1:c.97+2294G>C
ENST00000646375.1:c.*48C>G (AVPR2) ENSP00000496396.1:n.*48C>G
ENST00000337474.5:c.*48C>G (AVPR2) ENSP00000338072.5:n.*48C>G
ENST00000358927.6:c.*48C>G (AVPR2) ENSP00000351805.2:n.*48C>G
ENST00000370049.1:c.*340C>G (AVPR2) ENSP00000359066.1:n.*340C>G
ENST00000430697.1:c.1076C>G (AVPR2) ENSP00000393513.1:p.Ala359Gly
ENST00000434679.5:c.*530C>G (AVPR2) ENSP00000393397.1:n.*530C>G
ENST00000464967.5:n.154+2294G>C (L1CAM)
NM_000054.4:c.*48C>G (AVPR2) NP_000045.1:n.*48C>G
NM_001146151.1:c.*340C>G (AVPR2) NP_001139623.1:n.*340C>G
NR_027419.1:n.1211C>G (AVPR2)
XM_006724828.2:c.*48C>G (AVPR2) XP_006724891.1:n.*48C>G
NM_000054.5:c.*48C>G (AVPR2) NP_000045.1:n.*48C>G
NM_001146151.2:c.*340C>G (AVPR2) NP_001139623.1:n.*340C>G
XM_006724828.3:c.*48C>G (AVPR2) XP_006724891.1:n.*48C>G
NM_000054.6:c.*48C>G (AVPR2) NP_000045.1:n.*48C>G
NM_001146151.3:c.*340C>G (AVPR2) NP_001139623.1:n.*340C>G
NR_027419.2:n.1117C>G (AVPR2)
NM_000054.7:c.*48C>G (AVPR2) MANE Select NP_000045.1:n.*48C>G