Canonical Allele Identifier: CA2466520823

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906528C= , CM000685.2:g.153906528C= GRCh38
NC_000023.10:g.153171982C= , CM000685.1:g.153171982C= GRCh37
NC_000023.9:g.152825176C= NCBI36
NG_008687.1:g.6555C=
NG_009645.3:g.7696G=
NG_013220.1:g.24733G=

Transcript Alleles

HGVS Amino-acid change
ENST00000646375.2:c.916C= (AVPR2) MANE Select ENSP00000496396.1:p.Pro306=
ENST00000434679.6:c.*282C= (AVPR2) ENSP00000393397.1:n.*282C=
ENST00000642393.1:c.97+2542G=
ENST00000646191.1:c.97+2542G=
ENST00000646375.1:c.916C= (AVPR2) ENSP00000496396.1:p.Pro306=
ENST00000337474.5:c.916C= (AVPR2) ENSP00000338072.5:p.Pro306=
ENST00000358927.6:c.916C= (AVPR2) ENSP00000351805.2:p.Pro306=
ENST00000370049.1:c.*92C= (AVPR2) ENSP00000359066.1:n.*92C=
ENST00000430697.1:c.828C= (AVPR2) ENSP00000393513.1:p.Arg276=
ENST00000434679.5:c.*282C= (AVPR2) ENSP00000393397.1:n.*282C=
ENST00000464967.5:n.154+2542G= (L1CAM)
NM_000054.4:c.916C= (AVPR2) NP_000045.1:p.Pro306=
NM_001146151.1:c.*92C= (AVPR2) NP_001139623.1:n.*92C=
NR_027419.1:n.963C= (AVPR2)
XM_006724828.2:c.916C= (AVPR2) XP_006724891.1:p.Pro306=
NM_000054.5:c.916C= (AVPR2) NP_000045.1:p.Pro306=
NM_001146151.2:c.*92C= (AVPR2) NP_001139623.1:n.*92C=
XM_006724828.3:c.916C= (AVPR2) XP_006724891.1:p.Pro306=
NM_000054.6:c.916C= (AVPR2) NP_000045.1:p.Pro306=
NM_001146151.3:c.*92C= (AVPR2) NP_001139623.1:n.*92C=
NR_027419.2:n.869C= (AVPR2)
NM_000054.7:c.916C= (AVPR2) MANE Select NP_000045.1:p.Pro306=