Canonical Allele Identifier: CA415107331

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906087C>T , CM000685.2:g.153906087C>T GRCh38
NC_000023.10:g.153171541C>T , CM000685.1:g.153171541C>T GRCh37
NC_000023.9:g.152824735C>T NCBI36
NG_008687.1:g.6114C>T
NG_009645.3:g.8137G>A
NG_013220.1:g.25174G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.581C>T (AVPR2) MANE Select ENSP00000496396.1:p.Ala194Val
ENST00000434679.6:c.94C>T (AVPR2) ENSP00000393397.1:p.Pro32Ser
ENST00000642393.1:c.97+2983G>A
ENST00000646191.1:c.97+2983G>A
ENST00000646375.1:c.581C>T (AVPR2) ENSP00000496396.1:p.Ala194Val
ENST00000337474.5:c.581C>T (AVPR2) ENSP00000338072.5:p.Ala194Val
ENST00000358927.6:c.581C>T (AVPR2) ENSP00000351805.2:p.Ala194Val
ENST00000370049.1:c.581C>T (AVPR2) ENSP00000359066.1:p.Ala194Val
ENST00000430697.1:c.581C>T (AVPR2) ENSP00000393513.1:p.Ala194Val
ENST00000434679.5:c.94C>T (AVPR2) ENSP00000393397.1:p.Pro32Ser
ENST00000464967.5:n.154+2983G>A (L1CAM)
NM_000054.4:c.581C>T (AVPR2) NP_000045.1:p.Ala194Val
NM_001146151.1:c.581C>T (AVPR2) NP_001139623.1:p.Ala194Val
NR_027419.1:n.628C>T (AVPR2)
XM_006724828.2:c.581C>T (AVPR2) XP_006724891.1:p.Ala194Val
NM_000054.5:c.581C>T (AVPR2) NP_000045.1:p.Ala194Val
NM_001146151.2:c.581C>T (AVPR2) NP_001139623.1:p.Ala194Val
XM_006724828.3:c.581C>T (AVPR2) XP_006724891.1:p.Ala194Val
NM_000054.6:c.581C>T (AVPR2) NP_000045.1:p.Ala194Val
NM_001146151.3:c.581C>T (AVPR2) NP_001139623.1:p.Ala194Val
NR_027419.2:n.534C>T (AVPR2)
NM_000054.7:c.581C>T (AVPR2) MANE Select NP_000045.1:p.Ala194Val