Canonical Allele Identifier: CA2466520829

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906548G= , CM000685.2:g.153906548G= GRCh38
NC_000023.10:g.153172002G= , CM000685.1:g.153172002G= GRCh37
NC_000023.9:g.152825196G= NCBI36
NG_008687.1:g.6575G=
NG_009645.3:g.7676C=
NG_013220.1:g.24713C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.936G= (AVPR2) MANE Select ENSP00000496396.1:p.Leu312=
ENST00000434679.6:c.*302G= (AVPR2) ENSP00000393397.1:n.*302G=
ENST00000642393.1:c.97+2522C=
ENST00000646191.1:c.97+2522C=
ENST00000646375.1:c.936G= (AVPR2) ENSP00000496396.1:p.Leu312=
ENST00000337474.5:c.936G= (AVPR2) ENSP00000338072.5:p.Leu312=
ENST00000358927.6:c.936G= (AVPR2) ENSP00000351805.2:p.Leu312=
ENST00000370049.1:c.*112G= (AVPR2) ENSP00000359066.1:n.*112G=
ENST00000430697.1:c.848G= (AVPR2) ENSP00000393513.1:p.Cys283=
ENST00000434679.5:c.*302G= (AVPR2) ENSP00000393397.1:n.*302G=
ENST00000464967.5:n.154+2522C= (L1CAM)
NM_000054.4:c.936G= (AVPR2) NP_000045.1:p.Leu312=
NM_001146151.1:c.*112G= (AVPR2) NP_001139623.1:n.*112G=
NR_027419.1:n.983G= (AVPR2)
XM_006724828.2:c.936G= (AVPR2) XP_006724891.1:p.Leu312=
NM_000054.5:c.936G= (AVPR2) NP_000045.1:p.Leu312=
NM_001146151.2:c.*112G= (AVPR2) NP_001139623.1:n.*112G=
XM_006724828.3:c.936G= (AVPR2) XP_006724891.1:p.Leu312=
NM_000054.6:c.936G= (AVPR2) NP_000045.1:p.Leu312=
NM_001146151.3:c.*112G= (AVPR2) NP_001139623.1:n.*112G=
NR_027419.2:n.889G= (AVPR2)
NM_000054.7:c.936G= (AVPR2) MANE Select NP_000045.1:p.Leu312=