Canonical Allele Identifier: CA2579733585

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906816C>A , CM000685.2:g.153906816C>A GRCh38
NC_000023.10:g.153172270C>A , CM000685.1:g.153172270C>A GRCh37
NC_000023.9:g.152825464C>A NCBI36
NG_008687.1:g.6843C>A
NG_009645.3:g.7408G>T
NG_013220.1:g.24445G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*88C>A (AVPR2) MANE Select ENSP00000496396.1:n.*88C>A
ENST00000434679.6:c.*570C>A (AVPR2) ENSP00000393397.1:n.*570C>A
ENST00000642393.1:c.97+2254G>T
ENST00000646191.1:c.97+2254G>T
ENST00000646375.1:c.*88C>A (AVPR2) ENSP00000496396.1:n.*88C>A
ENST00000337474.5:c.*88C>A (AVPR2) ENSP00000338072.5:n.*88C>A
ENST00000358927.6:c.*88C>A (AVPR2) ENSP00000351805.2:n.*88C>A
ENST00000430697.1:c.1116C>A (AVPR2) ENSP00000393513.1:p.Thr372=
ENST00000434679.5:c.*570C>A (AVPR2) ENSP00000393397.1:n.*570C>A
ENST00000464967.5:n.154+2254G>T (L1CAM)
NM_000054.4:c.*88C>A (AVPR2) NP_000045.1:n.*88C>A
NM_001146151.1:c.*380C>A (AVPR2) NP_001139623.1:n.*380C>A
NR_027419.1:n.1251C>A (AVPR2)
XM_006724828.2:c.*88C>A (AVPR2) XP_006724891.1:n.*88C>A
NM_000054.5:c.*88C>A (AVPR2) NP_000045.1:n.*88C>A
NM_001146151.2:c.*380C>A (AVPR2) NP_001139623.1:n.*380C>A
XM_006724828.3:c.*88C>A (AVPR2) XP_006724891.1:n.*88C>A
NM_000054.6:c.*88C>A (AVPR2) NP_000045.1:n.*88C>A
NM_001146151.3:c.*380C>A (AVPR2) NP_001139623.1:n.*380C>A
NR_027419.2:n.1157C>A (AVPR2)
NM_000054.7:c.*88C>A (AVPR2) MANE Select NP_000045.1:n.*88C>A