Canonical Allele Identifier: CA2466520917

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906782T= , CM000685.2:g.153906782T= GRCh38
NC_000023.10:g.153172236T= , CM000685.1:g.153172236T= GRCh37
NC_000023.9:g.152825430T= NCBI36
NG_008687.1:g.6809T=
NG_009645.3:g.7442A=
NG_013220.1:g.24479A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*54T= (AVPR2) MANE Select ENSP00000496396.1:n.*54T=
ENST00000434679.6:c.*536T= (AVPR2) ENSP00000393397.1:n.*536T=
ENST00000642393.1:c.97+2288A=
ENST00000646191.1:c.97+2288A=
ENST00000646375.1:c.*54T= (AVPR2) ENSP00000496396.1:n.*54T=
ENST00000337474.5:c.*54T= (AVPR2) ENSP00000338072.5:n.*54T=
ENST00000358927.6:c.*54T= (AVPR2) ENSP00000351805.2:n.*54T=
ENST00000430697.1:c.1082T= (AVPR2) ENSP00000393513.1:p.Leu361=
ENST00000434679.5:c.*536T= (AVPR2) ENSP00000393397.1:n.*536T=
ENST00000464967.5:n.154+2288A= (L1CAM)
NM_000054.4:c.*54T= (AVPR2) NP_000045.1:n.*54T=
NM_001146151.1:c.*346T= (AVPR2) NP_001139623.1:n.*346T=
NR_027419.1:n.1217T= (AVPR2)
XM_006724828.2:c.*54T= (AVPR2) XP_006724891.1:n.*54T=
NM_000054.5:c.*54T= (AVPR2) NP_000045.1:n.*54T=
NM_001146151.2:c.*346T= (AVPR2) NP_001139623.1:n.*346T=
XM_006724828.3:c.*54T= (AVPR2) XP_006724891.1:n.*54T=
NM_000054.6:c.*54T= (AVPR2) NP_000045.1:n.*54T=
NM_001146151.3:c.*346T= (AVPR2) NP_001139623.1:n.*346T=
NR_027419.2:n.1123T= (AVPR2)
NM_000054.7:c.*54T= (AVPR2) MANE Select NP_000045.1:n.*54T=