Canonical Allele Identifier: CA415111604

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906647A>C , CM000685.2:g.153906647A>C GRCh38
NC_000023.10:g.153172101A>C , CM000685.1:g.153172101A>C GRCh37
NC_000023.9:g.152825295A>C NCBI36
NG_008687.1:g.6674A>C
NG_009645.3:g.7577T>G
NG_013220.1:g.24614T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.1035A>C (AVPR2) MANE Select ENSP00000496396.1:p.Gly345=
ENST00000434679.6:c.*401A>C (AVPR2) ENSP00000393397.1:n.*401A>C
ENST00000642393.1:c.97+2423T>G
ENST00000646191.1:c.97+2423T>G
ENST00000646375.1:c.1035A>C (AVPR2) ENSP00000496396.1:p.Gly345=
ENST00000337474.5:c.1035A>C (AVPR2) ENSP00000338072.5:p.Gly345=
ENST00000358927.6:c.1035A>C (AVPR2) ENSP00000351805.2:p.Gly345=
ENST00000370049.1:c.*211A>C (AVPR2) ENSP00000359066.1:n.*211A>C
ENST00000430697.1:c.947A>C (AVPR2) ENSP00000393513.1:p.Asp316Ala
ENST00000434679.5:c.*401A>C (AVPR2) ENSP00000393397.1:n.*401A>C
ENST00000464967.5:n.154+2423T>G (L1CAM)
NM_000054.4:c.1035A>C (AVPR2) NP_000045.1:p.Gly345=
NM_001146151.1:c.*211A>C (AVPR2) NP_001139623.1:n.*211A>C
NR_027419.1:n.1082A>C (AVPR2)
XM_006724828.2:c.1035A>C (AVPR2) XP_006724891.1:p.Gly345=
NM_000054.5:c.1035A>C (AVPR2) NP_000045.1:p.Gly345=
NM_001146151.2:c.*211A>C (AVPR2) NP_001139623.1:n.*211A>C
XM_006724828.3:c.1035A>C (AVPR2) XP_006724891.1:p.Gly345=
NM_000054.6:c.1035A>C (AVPR2) NP_000045.1:p.Gly345=
NM_001146151.3:c.*211A>C (AVPR2) NP_001139623.1:n.*211A>C
NR_027419.2:n.988A>C (AVPR2)
NM_000054.7:c.1035A>C (AVPR2) MANE Select NP_000045.1:p.Gly345=