Canonical Allele Identifier: CA2466520378

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153905394C= , CM000685.2:g.153905394C= GRCh38
NC_000023.10:g.153170848C= , CM000685.1:g.153170848C= GRCh37
NC_000023.9:g.152824042C= NCBI36
NG_008687.1:g.5421C=
NG_009645.3:g.8830G=
NG_013220.1:g.25867G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.26-138C= (AVPR2) MANE Select ENSP00000496396.1:n.26-138C=
ENST00000434679.6:c.25+224C= (AVPR2) ENSP00000393397.1:n.25+224C=
ENST00000642393.1:c.97+3676G=
ENST00000646191.1:c.97+3676G=
ENST00000646375.1:c.26-138C= (AVPR2) ENSP00000496396.1:n.26-138C=
ENST00000337474.5:c.26-138C= (AVPR2) ENSP00000338072.5:n.26-138C=
ENST00000358927.6:c.26-138C= (AVPR2) ENSP00000351805.2:n.26-138C=
ENST00000370049.1:c.26-138C= (AVPR2) ENSP00000359066.1:n.26-138C=
ENST00000430697.1:c.26-138C= (AVPR2) ENSP00000393513.1:n.26-138C=
ENST00000434679.5:c.25+224C= (AVPR2) ENSP00000393397.1:n.25+224C=
ENST00000464967.5:n.154+3676G= (L1CAM)
NM_000054.4:c.26-138C= (AVPR2) NP_000045.1:n.26-138C=
NM_001146151.1:c.26-138C= (AVPR2) NP_001139623.1:n.26-138C=
NR_027419.1:n.559+224C= (AVPR2)
XM_006724828.2:c.26-138C= (AVPR2) XP_006724891.1:n.26-138C=
NM_000054.5:c.26-138C= (AVPR2) NP_000045.1:n.26-138C=
NM_001146151.2:c.26-138C= (AVPR2) NP_001139623.1:n.26-138C=
XM_006724828.3:c.26-138C= (AVPR2) XP_006724891.1:n.26-138C=
NM_000054.6:c.26-138C= (AVPR2) NP_000045.1:n.26-138C=
NM_001146151.3:c.26-138C= (AVPR2) NP_001139623.1:n.26-138C=
NR_027419.2:n.465+224C= (AVPR2)
NM_000054.7:c.26-138C= (AVPR2) MANE Select NP_000045.1:n.26-138C=