Canonical Allele Identifier: CA415111825

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906666G>T , CM000685.2:g.153906666G>T GRCh38
NC_000023.10:g.153172120G>T , CM000685.1:g.153172120G>T GRCh37
NC_000023.9:g.152825314G>T NCBI36
NG_008687.1:g.6693G>T
NG_009645.3:g.7558C>A
NG_013220.1:g.24595C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.1054G>T (AVPR2) MANE Select ENSP00000496396.1:p.Gly352Cys
ENST00000434679.6:c.*420G>T (AVPR2) ENSP00000393397.1:n.*420G>T
ENST00000642393.1:c.97+2404C>A
ENST00000646191.1:c.97+2404C>A
ENST00000646375.1:c.1054G>T (AVPR2) ENSP00000496396.1:p.Gly352Cys
ENST00000337474.5:c.1054G>T (AVPR2) ENSP00000338072.5:p.Gly352Cys
ENST00000358927.6:c.1054G>T (AVPR2) ENSP00000351805.2:p.Gly352Cys
ENST00000370049.1:c.*230G>T (AVPR2) ENSP00000359066.1:n.*230G>T
ENST00000430697.1:c.966G>T (AVPR2) ENSP00000393513.1:p.Trp322Cys
ENST00000434679.5:c.*420G>T (AVPR2) ENSP00000393397.1:n.*420G>T
ENST00000464967.5:n.154+2404C>A (L1CAM)
NM_000054.4:c.1054G>T (AVPR2) NP_000045.1:p.Gly352Cys
NM_001146151.1:c.*230G>T (AVPR2) NP_001139623.1:n.*230G>T
NR_027419.1:n.1101G>T (AVPR2)
XM_006724828.2:c.1054G>T (AVPR2) XP_006724891.1:p.Gly352Cys
NM_000054.5:c.1054G>T (AVPR2) NP_000045.1:p.Gly352Cys
NM_001146151.2:c.*230G>T (AVPR2) NP_001139623.1:n.*230G>T
XM_006724828.3:c.1054G>T (AVPR2) XP_006724891.1:p.Gly352Cys
NM_000054.6:c.1054G>T (AVPR2) NP_000045.1:p.Gly352Cys
NM_001146151.3:c.*230G>T (AVPR2) NP_001139623.1:n.*230G>T
NR_027419.2:n.1007G>T (AVPR2)
NM_000054.7:c.1054G>T (AVPR2) MANE Select NP_000045.1:p.Gly352Cys