Canonical Allele Identifier: CA415112560

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906770C>A , CM000685.2:g.153906770C>A GRCh38
NC_000023.10:g.153172224C>A , CM000685.1:g.153172224C>A GRCh37
NC_000023.9:g.152825418C>A NCBI36
NG_008687.1:g.6797C>A
NG_009645.3:g.7454G>T
NG_013220.1:g.24491G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*42C>A (AVPR2) MANE Select ENSP00000496396.1:n.*42C>A
ENST00000434679.6:c.*524C>A (AVPR2) ENSP00000393397.1:n.*524C>A
ENST00000642393.1:c.97+2300G>T
ENST00000646191.1:c.97+2300G>T
ENST00000646375.1:c.*42C>A (AVPR2) ENSP00000496396.1:n.*42C>A
ENST00000337474.5:c.*42C>A (AVPR2) ENSP00000338072.5:n.*42C>A
ENST00000358927.6:c.*42C>A (AVPR2) ENSP00000351805.2:n.*42C>A
ENST00000370049.1:c.*334C>A (AVPR2) ENSP00000359066.1:n.*334C>A
ENST00000430697.1:c.1070C>A (AVPR2) ENSP00000393513.1:p.Ser357Ter
ENST00000434679.5:c.*524C>A (AVPR2) ENSP00000393397.1:n.*524C>A
ENST00000464967.5:n.154+2300G>T (L1CAM)
NM_000054.4:c.*42C>A (AVPR2) NP_000045.1:n.*42C>A
NM_001146151.1:c.*334C>A (AVPR2) NP_001139623.1:n.*334C>A
NR_027419.1:n.1205C>A (AVPR2)
XM_006724828.2:c.*42C>A (AVPR2) XP_006724891.1:n.*42C>A
NM_000054.5:c.*42C>A (AVPR2) NP_000045.1:n.*42C>A
NM_001146151.2:c.*334C>A (AVPR2) NP_001139623.1:n.*334C>A
XM_006724828.3:c.*42C>A (AVPR2) XP_006724891.1:n.*42C>A
NM_000054.6:c.*42C>A (AVPR2) NP_000045.1:n.*42C>A
NM_001146151.3:c.*334C>A (AVPR2) NP_001139623.1:n.*334C>A
NR_027419.2:n.1111C>A (AVPR2)
NM_000054.7:c.*42C>A (AVPR2) MANE Select NP_000045.1:n.*42C>A