Canonical Allele Identifier: CA2695073690

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906834A>C , CM000685.2:g.153906834A>C GRCh38
NC_000023.10:g.153172288A>C , CM000685.1:g.153172288A>C GRCh37
NC_000023.9:g.152825482A>C NCBI36
NG_008687.1:g.6861A>C
NG_009645.3:g.7390T>G
NG_013220.1:g.24427T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*106A>C (AVPR2) MANE Select ENSP00000496396.1:n.*106A>C
ENST00000434679.6:c.*588A>C (AVPR2) ENSP00000393397.1:n.*588A>C
ENST00000642393.1:c.97+2236T>G
ENST00000646191.1:c.97+2236T>G
ENST00000646375.1:c.*106A>C (AVPR2) ENSP00000496396.1:n.*106A>C
ENST00000337474.5:c.*106A>C (AVPR2) ENSP00000338072.5:n.*106A>C
ENST00000358927.6:c.*106A>C (AVPR2) ENSP00000351805.2:n.*106A>C
ENST00000434679.5:c.*588A>C (AVPR2) ENSP00000393397.1:n.*588A>C
ENST00000464967.5:n.154+2236T>G (L1CAM)
NM_000054.4:c.*106A>C (AVPR2) NP_000045.1:n.*106A>C
NM_001146151.1:c.*398A>C (AVPR2) NP_001139623.1:n.*398A>C
NR_027419.1:n.1269A>C (AVPR2)
XM_006724828.2:c.*106A>C (AVPR2) XP_006724891.1:n.*106A>C
NM_000054.5:c.*106A>C (AVPR2) NP_000045.1:n.*106A>C
NM_001146151.2:c.*398A>C (AVPR2) NP_001139623.1:n.*398A>C
XM_006724828.3:c.*106A>C (AVPR2) XP_006724891.1:n.*106A>C
NM_000054.6:c.*106A>C (AVPR2) NP_000045.1:n.*106A>C
NM_001146151.3:c.*398A>C (AVPR2) NP_001139623.1:n.*398A>C
NR_027419.2:n.1175A>C (AVPR2)
NM_000054.7:c.*106A>C (AVPR2) MANE Select NP_000045.1:n.*106A>C