Canonical Allele Identifier: CA2570695047

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906820G>T , CM000685.2:g.153906820G>T GRCh38
NC_000023.10:g.153172274G>T , CM000685.1:g.153172274G>T GRCh37
NC_000023.9:g.152825468G>T NCBI36
NG_008687.1:g.6847G>T
NG_009645.3:g.7404C>A
NG_013220.1:g.24441C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*92G>T (AVPR2) MANE Select ENSP00000496396.1:n.*92G>T
ENST00000434679.6:c.*574G>T (AVPR2) ENSP00000393397.1:n.*574G>T
ENST00000642393.1:c.97+2250C>A
ENST00000646191.1:c.97+2250C>A
ENST00000646375.1:c.*92G>T (AVPR2) ENSP00000496396.1:n.*92G>T
ENST00000337474.5:c.*92G>T (AVPR2) ENSP00000338072.5:n.*92G>T
ENST00000358927.6:c.*92G>T (AVPR2) ENSP00000351805.2:n.*92G>T
ENST00000434679.5:c.*574G>T (AVPR2) ENSP00000393397.1:n.*574G>T
ENST00000464967.5:n.154+2250C>A (L1CAM)
NM_000054.4:c.*92G>T (AVPR2) NP_000045.1:n.*92G>T
NM_001146151.1:c.*384G>T (AVPR2) NP_001139623.1:n.*384G>T
NR_027419.1:n.1255G>T (AVPR2)
XM_006724828.2:c.*92G>T (AVPR2) XP_006724891.1:n.*92G>T
NM_000054.5:c.*92G>T (AVPR2) NP_000045.1:n.*92G>T
NM_001146151.2:c.*384G>T (AVPR2) NP_001139623.1:n.*384G>T
XM_006724828.3:c.*92G>T (AVPR2) XP_006724891.1:n.*92G>T
NM_000054.6:c.*92G>T (AVPR2) NP_000045.1:n.*92G>T
NM_001146151.3:c.*384G>T (AVPR2) NP_001139623.1:n.*384G>T
NR_027419.2:n.1161G>T (AVPR2)
NM_000054.7:c.*92G>T (AVPR2) MANE Select NP_000045.1:n.*92G>T