Canonical Allele Identifier: CA415112577

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906772G>T , CM000685.2:g.153906772G>T GRCh38
NC_000023.10:g.153172226G>T , CM000685.1:g.153172226G>T GRCh37
NC_000023.9:g.152825420G>T NCBI36
NG_008687.1:g.6799G>T
NG_009645.3:g.7452C>A
NG_013220.1:g.24489C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*44G>T (AVPR2) MANE Select ENSP00000496396.1:n.*44G>T
ENST00000434679.6:c.*526G>T (AVPR2) ENSP00000393397.1:n.*526G>T
ENST00000642393.1:c.97+2298C>A
ENST00000646191.1:c.97+2298C>A
ENST00000646375.1:c.*44G>T (AVPR2) ENSP00000496396.1:n.*44G>T
ENST00000337474.5:c.*44G>T (AVPR2) ENSP00000338072.5:n.*44G>T
ENST00000358927.6:c.*44G>T (AVPR2) ENSP00000351805.2:n.*44G>T
ENST00000370049.1:c.*336G>T (AVPR2) ENSP00000359066.1:n.*336G>T
ENST00000430697.1:c.1072G>T (AVPR2) ENSP00000393513.1:p.Ala358Ser
ENST00000434679.5:c.*526G>T (AVPR2) ENSP00000393397.1:n.*526G>T
ENST00000464967.5:n.154+2298C>A (L1CAM)
NM_000054.4:c.*44G>T (AVPR2) NP_000045.1:n.*44G>T
NM_001146151.1:c.*336G>T (AVPR2) NP_001139623.1:n.*336G>T
NR_027419.1:n.1207G>T (AVPR2)
XM_006724828.2:c.*44G>T (AVPR2) XP_006724891.1:n.*44G>T
NM_000054.5:c.*44G>T (AVPR2) NP_000045.1:n.*44G>T
NM_001146151.2:c.*336G>T (AVPR2) NP_001139623.1:n.*336G>T
XM_006724828.3:c.*44G>T (AVPR2) XP_006724891.1:n.*44G>T
NM_000054.6:c.*44G>T (AVPR2) NP_000045.1:n.*44G>T
NM_001146151.3:c.*336G>T (AVPR2) NP_001139623.1:n.*336G>T
NR_027419.2:n.1113G>T (AVPR2)
NM_000054.7:c.*44G>T (AVPR2) MANE Select NP_000045.1:n.*44G>T