Canonical Allele Identifier: CA415112268

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906729G>T , CM000685.2:g.153906729G>T GRCh38
NC_000023.10:g.153172183G>T , CM000685.1:g.153172183G>T GRCh37
NC_000023.9:g.152825377G>T NCBI36
NG_008687.1:g.6756G>T
NG_009645.3:g.7495C>A
NG_013220.1:g.24532C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*1G>T (AVPR2) MANE Select ENSP00000496396.1:n.*1G>T
ENST00000434679.6:c.*483G>T (AVPR2) ENSP00000393397.1:n.*483G>T
ENST00000642393.1:c.97+2341C>A
ENST00000646191.1:c.97+2341C>A
ENST00000646375.1:c.*1G>T (AVPR2) ENSP00000496396.1:n.*1G>T
ENST00000337474.5:c.*1G>T (AVPR2) ENSP00000338072.5:n.*1G>T
ENST00000358927.6:c.*1G>T (AVPR2) ENSP00000351805.2:n.*1G>T
ENST00000370049.1:c.*293G>T (AVPR2) ENSP00000359066.1:n.*293G>T
ENST00000430697.1:c.1029G>T (AVPR2) ENSP00000393513.1:p.Glu343Asp
ENST00000434679.5:c.*483G>T (AVPR2) ENSP00000393397.1:n.*483G>T
ENST00000464967.5:n.154+2341C>A (L1CAM)
NM_000054.4:c.*1G>T (AVPR2) NP_000045.1:n.*1G>T
NM_001146151.1:c.*293G>T (AVPR2) NP_001139623.1:n.*293G>T
NR_027419.1:n.1164G>T (AVPR2)
XM_006724828.2:c.*1G>T (AVPR2) XP_006724891.1:n.*1G>T
NM_000054.5:c.*1G>T (AVPR2) NP_000045.1:n.*1G>T
NM_001146151.2:c.*293G>T (AVPR2) NP_001139623.1:n.*293G>T
XM_006724828.3:c.*1G>T (AVPR2) XP_006724891.1:n.*1G>T
NM_000054.6:c.*1G>T (AVPR2) NP_000045.1:n.*1G>T
NM_001146151.3:c.*293G>T (AVPR2) NP_001139623.1:n.*293G>T
NR_027419.2:n.1070G>T (AVPR2)
NM_000054.7:c.*1G>T (AVPR2) MANE Select NP_000045.1:n.*1G>T