Canonical Allele Identifier: CA2466520934

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906830C= , CM000685.2:g.153906830C= GRCh38
NC_000023.10:g.153172284C= , CM000685.1:g.153172284C= GRCh37
NC_000023.9:g.152825478C= NCBI36
NG_008687.1:g.6857C=
NG_009645.3:g.7394G=
NG_013220.1:g.24431G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*102C= (AVPR2) MANE Select ENSP00000496396.1:n.*102C=
ENST00000434679.6:c.*584C= (AVPR2) ENSP00000393397.1:n.*584C=
ENST00000642393.1:c.97+2240G=
ENST00000646191.1:c.97+2240G=
ENST00000646375.1:c.*102C= (AVPR2) ENSP00000496396.1:n.*102C=
ENST00000337474.5:c.*102C= (AVPR2) ENSP00000338072.5:n.*102C=
ENST00000358927.6:c.*102C= (AVPR2) ENSP00000351805.2:n.*102C=
ENST00000434679.5:c.*584C= (AVPR2) ENSP00000393397.1:n.*584C=
ENST00000464967.5:n.154+2240G= (L1CAM)
NM_000054.4:c.*102C= (AVPR2) NP_000045.1:n.*102C=
NM_001146151.1:c.*394C= (AVPR2) NP_001139623.1:n.*394C=
NR_027419.1:n.1265C= (AVPR2)
XM_006724828.2:c.*102C= (AVPR2) XP_006724891.1:n.*102C=
NM_000054.5:c.*102C= (AVPR2) NP_000045.1:n.*102C=
NM_001146151.2:c.*394C= (AVPR2) NP_001139623.1:n.*394C=
XM_006724828.3:c.*102C= (AVPR2) XP_006724891.1:n.*102C=
NM_000054.6:c.*102C= (AVPR2) NP_000045.1:n.*102C=
NM_001146151.3:c.*394C= (AVPR2) NP_001139623.1:n.*394C=
NR_027419.2:n.1171C= (AVPR2)
NM_000054.7:c.*102C= (AVPR2) MANE Select NP_000045.1:n.*102C=