Canonical Allele Identifier: CA2466520781

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906400G= , CM000685.2:g.153906400G= GRCh38
NC_000023.10:g.153171854G= , CM000685.1:g.153171854G= GRCh37
NC_000023.9:g.152825048G= NCBI36
NG_008687.1:g.6427G=
NG_009645.3:g.7824C=
NG_013220.1:g.24861C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.894G= (AVPR2) MANE Select ENSP00000496396.1:p.Pro298=
ENST00000434679.6:c.*260G= (AVPR2) ENSP00000393397.1:n.*260G=
ENST00000642393.1:c.97+2670C=
ENST00000646191.1:c.97+2670C=
ENST00000646375.1:c.894G= (AVPR2) ENSP00000496396.1:p.Pro298=
ENST00000337474.5:c.894G= (AVPR2) ENSP00000338072.5:p.Pro298=
ENST00000358927.6:c.894G= (AVPR2) ENSP00000351805.2:p.Pro298=
ENST00000370049.1:c.894G= (AVPR2) ENSP00000359066.1:p.Pro298=
ENST00000430697.1:c.822+72G= (AVPR2) ENSP00000393513.1:n.822+72G=
ENST00000434679.5:c.*260G= (AVPR2) ENSP00000393397.1:n.*260G=
ENST00000464967.5:n.154+2670C= (L1CAM)
NM_000054.4:c.894G= (AVPR2) NP_000045.1:p.Pro298=
NM_001146151.1:c.894G= (AVPR2) NP_001139623.1:p.Pro298=
NR_027419.1:n.941G= (AVPR2)
XM_006724828.2:c.894G= (AVPR2) XP_006724891.1:p.Pro298=
NM_000054.5:c.894G= (AVPR2) NP_000045.1:p.Pro298=
NM_001146151.2:c.894G= (AVPR2) NP_001139623.1:p.Pro298=
XM_006724828.3:c.894G= (AVPR2) XP_006724891.1:p.Pro298=
NM_000054.6:c.894G= (AVPR2) NP_000045.1:p.Pro298=
NM_001146151.3:c.894G= (AVPR2) NP_001139623.1:p.Pro298=
NR_027419.2:n.847G= (AVPR2)
NM_000054.7:c.894G= (AVPR2) MANE Select NP_000045.1:p.Pro298=