Canonical Allele Identifier: CA415112776

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906803C>A , CM000685.2:g.153906803C>A GRCh38
NC_000023.10:g.153172257C>A , CM000685.1:g.153172257C>A GRCh37
NC_000023.9:g.152825451C>A NCBI36
NG_008687.1:g.6830C>A
NG_009645.3:g.7421G>T
NG_013220.1:g.24458G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*75C>A (AVPR2) MANE Select ENSP00000496396.1:n.*75C>A
ENST00000434679.6:c.*557C>A (AVPR2) ENSP00000393397.1:n.*557C>A
ENST00000642393.1:c.97+2267G>T
ENST00000646191.1:c.97+2267G>T
ENST00000646375.1:c.*75C>A (AVPR2) ENSP00000496396.1:n.*75C>A
ENST00000337474.5:c.*75C>A (AVPR2) ENSP00000338072.5:n.*75C>A
ENST00000358927.6:c.*75C>A (AVPR2) ENSP00000351805.2:n.*75C>A
ENST00000430697.1:c.1103C>A (AVPR2) ENSP00000393513.1:p.Thr368Asn
ENST00000434679.5:c.*557C>A (AVPR2) ENSP00000393397.1:n.*557C>A
ENST00000464967.5:n.154+2267G>T (L1CAM)
NM_000054.4:c.*75C>A (AVPR2) NP_000045.1:n.*75C>A
NM_001146151.1:c.*367C>A (AVPR2) NP_001139623.1:n.*367C>A
NR_027419.1:n.1238C>A (AVPR2)
XM_006724828.2:c.*75C>A (AVPR2) XP_006724891.1:n.*75C>A
NM_000054.5:c.*75C>A (AVPR2) NP_000045.1:n.*75C>A
NM_001146151.2:c.*367C>A (AVPR2) NP_001139623.1:n.*367C>A
XM_006724828.3:c.*75C>A (AVPR2) XP_006724891.1:n.*75C>A
NM_000054.6:c.*75C>A (AVPR2) NP_000045.1:n.*75C>A
NM_001146151.3:c.*367C>A (AVPR2) NP_001139623.1:n.*367C>A
NR_027419.2:n.1144C>A (AVPR2)
NM_000054.7:c.*75C>A (AVPR2) MANE Select NP_000045.1:n.*75C>A