Canonical Allele Identifier: CA2695073704

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906853G>T , CM000685.2:g.153906853G>T GRCh38
NC_000023.10:g.153172307G>T , CM000685.1:g.153172307G>T GRCh37
NC_000023.9:g.152825501G>T NCBI36
NG_008687.1:g.6880G>T
NG_009645.3:g.7371C>A
NG_013220.1:g.24408C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*125G>T (AVPR2) MANE Select ENSP00000496396.1:n.*125G>T
ENST00000434679.6:c.*607G>T (AVPR2) ENSP00000393397.1:n.*607G>T
ENST00000642393.1:c.97+2217C>A
ENST00000646191.1:c.97+2217C>A
ENST00000646375.1:c.*125G>T (AVPR2) ENSP00000496396.1:n.*125G>T
ENST00000337474.5:c.*125G>T (AVPR2) ENSP00000338072.5:n.*125G>T
ENST00000358927.6:c.*125G>T (AVPR2) ENSP00000351805.2:n.*125G>T
ENST00000434679.5:c.*607G>T (AVPR2) ENSP00000393397.1:n.*607G>T
ENST00000464967.5:n.154+2217C>A (L1CAM)
NM_000054.4:c.*125G>T (AVPR2) NP_000045.1:n.*125G>T
NM_001146151.1:c.*417G>T (AVPR2) NP_001139623.1:n.*417G>T
NR_027419.1:n.1288G>T (AVPR2)
XM_006724828.2:c.*125G>T (AVPR2) XP_006724891.1:n.*125G>T
NM_000054.5:c.*125G>T (AVPR2) NP_000045.1:n.*125G>T
NM_001146151.2:c.*417G>T (AVPR2) NP_001139623.1:n.*417G>T
XM_006724828.3:c.*125G>T (AVPR2) XP_006724891.1:n.*125G>T
NM_000054.6:c.*125G>T (AVPR2) NP_000045.1:n.*125G>T
NM_001146151.3:c.*417G>T (AVPR2) NP_001139623.1:n.*417G>T
NR_027419.2:n.1194G>T (AVPR2)
NM_000054.7:c.*125G>T (AVPR2) MANE Select NP_000045.1:n.*125G>T