Canonical Allele Identifier: CA415112400

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906751C>G , CM000685.2:g.153906751C>G GRCh38
NC_000023.10:g.153172205C>G , CM000685.1:g.153172205C>G GRCh37
NC_000023.9:g.152825399C>G NCBI36
NG_008687.1:g.6778C>G
NG_009645.3:g.7473G>C
NG_013220.1:g.24510G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*23C>G (AVPR2) MANE Select ENSP00000496396.1:n.*23C>G
ENST00000434679.6:c.*505C>G (AVPR2) ENSP00000393397.1:n.*505C>G
ENST00000642393.1:c.97+2319G>C
ENST00000646191.1:c.97+2319G>C
ENST00000646375.1:c.*23C>G (AVPR2) ENSP00000496396.1:n.*23C>G
ENST00000337474.5:c.*23C>G (AVPR2) ENSP00000338072.5:n.*23C>G
ENST00000358927.6:c.*23C>G (AVPR2) ENSP00000351805.2:n.*23C>G
ENST00000370049.1:c.*315C>G (AVPR2) ENSP00000359066.1:n.*315C>G
ENST00000430697.1:c.1051C>G (AVPR2) ENSP00000393513.1:p.Leu351Val
ENST00000434679.5:c.*505C>G (AVPR2) ENSP00000393397.1:n.*505C>G
ENST00000464967.5:n.154+2319G>C (L1CAM)
NM_000054.4:c.*23C>G (AVPR2) NP_000045.1:n.*23C>G
NM_001146151.1:c.*315C>G (AVPR2) NP_001139623.1:n.*315C>G
NR_027419.1:n.1186C>G (AVPR2)
XM_006724828.2:c.*23C>G (AVPR2) XP_006724891.1:n.*23C>G
NM_000054.5:c.*23C>G (AVPR2) NP_000045.1:n.*23C>G
NM_001146151.2:c.*315C>G (AVPR2) NP_001139623.1:n.*315C>G
XM_006724828.3:c.*23C>G (AVPR2) XP_006724891.1:n.*23C>G
NM_000054.6:c.*23C>G (AVPR2) NP_000045.1:n.*23C>G
NM_001146151.3:c.*315C>G (AVPR2) NP_001139623.1:n.*315C>G
NR_027419.2:n.1092C>G (AVPR2)
NM_000054.7:c.*23C>G (AVPR2) MANE Select NP_000045.1:n.*23C>G