Canonical Allele Identifier: CA2466520935

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906833G= , CM000685.2:g.153906833G= GRCh38
NC_000023.10:g.153172287G= , CM000685.1:g.153172287G= GRCh37
NC_000023.9:g.152825481G= NCBI36
NG_008687.1:g.6860G=
NG_009645.3:g.7391C=
NG_013220.1:g.24428C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*105G= (AVPR2) MANE Select ENSP00000496396.1:n.*105G=
ENST00000434679.6:c.*587G= (AVPR2) ENSP00000393397.1:n.*587G=
ENST00000642393.1:c.97+2237C=
ENST00000646191.1:c.97+2237C=
ENST00000646375.1:c.*105G= (AVPR2) ENSP00000496396.1:n.*105G=
ENST00000337474.5:c.*105G= (AVPR2) ENSP00000338072.5:n.*105G=
ENST00000358927.6:c.*105G= (AVPR2) ENSP00000351805.2:n.*105G=
ENST00000434679.5:c.*587G= (AVPR2) ENSP00000393397.1:n.*587G=
ENST00000464967.5:n.154+2237C= (L1CAM)
NM_000054.4:c.*105G= (AVPR2) NP_000045.1:n.*105G=
NM_001146151.1:c.*397G= (AVPR2) NP_001139623.1:n.*397G=
NR_027419.1:n.1268G= (AVPR2)
XM_006724828.2:c.*105G= (AVPR2) XP_006724891.1:n.*105G=
NM_000054.5:c.*105G= (AVPR2) NP_000045.1:n.*105G=
NM_001146151.2:c.*397G= (AVPR2) NP_001139623.1:n.*397G=
XM_006724828.3:c.*105G= (AVPR2) XP_006724891.1:n.*105G=
NM_000054.6:c.*105G= (AVPR2) NP_000045.1:n.*105G=
NM_001146151.3:c.*397G= (AVPR2) NP_001139623.1:n.*397G=
NR_027419.2:n.1174G= (AVPR2)
NM_000054.7:c.*105G= (AVPR2) MANE Select NP_000045.1:n.*105G=