Canonical Allele Identifier: CA2466520333

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153905266G= , CM000685.2:g.153905266G= GRCh38
NC_000023.10:g.153170720G= , CM000685.1:g.153170720G= GRCh37
NC_000023.9:g.152823914G= NCBI36
NG_008687.1:g.5293G=
NG_009645.3:g.8958C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.25+96G= (AVPR2) MANE Select ENSP00000496396.1:n.25+96G=
ENST00000434679.6:c.25+96G= (AVPR2) ENSP00000393397.1:n.25+96G=
ENST00000642393.1:c.97+3804C=
ENST00000646191.1:c.97+3804C=
ENST00000646375.1:c.25+96G= (AVPR2) ENSP00000496396.1:n.25+96G=
ENST00000337474.5:c.25+96G= (AVPR2) ENSP00000338072.5:n.25+96G=
ENST00000358927.6:c.25+96G= (AVPR2) ENSP00000351805.2:n.25+96G=
ENST00000370049.1:c.25+96G= (AVPR2) ENSP00000359066.1:n.25+96G=
ENST00000430697.1:c.25+96G= (AVPR2) ENSP00000393513.1:n.25+96G=
ENST00000434679.5:c.25+96G= (AVPR2) ENSP00000393397.1:n.25+96G=
ENST00000464967.5:n.154+3804C= (L1CAM)
NM_000054.4:c.25+96G= (AVPR2) NP_000045.1:n.25+96G=
NM_001146151.1:c.25+96G= (AVPR2) NP_001139623.1:n.25+96G=
NR_027419.1:n.559+96G= (AVPR2)
XM_006724828.2:c.25+96G= (AVPR2) XP_006724891.1:n.25+96G=
NM_000054.5:c.25+96G= (AVPR2) NP_000045.1:n.25+96G=
NM_001146151.2:c.25+96G= (AVPR2) NP_001139623.1:n.25+96G=
XM_006724828.3:c.25+96G= (AVPR2) XP_006724891.1:n.25+96G=
NM_000054.6:c.25+96G= (AVPR2) NP_000045.1:n.25+96G=
NM_001146151.3:c.25+96G= (AVPR2) NP_001139623.1:n.25+96G=
NR_027419.2:n.465+96G= (AVPR2)
NM_000054.7:c.25+96G= (AVPR2) MANE Select NP_000045.1:n.25+96G=