Canonical Allele Identifier: CA2466520460

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153905581G= , CM000685.2:g.153905581G= GRCh38
NC_000023.10:g.153171035G= , CM000685.1:g.153171035G= GRCh37
NC_000023.9:g.152824229G= NCBI36
NG_008687.1:g.5608G=
NG_009645.3:g.8643C=
NG_013220.1:g.25680C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.75G= (AVPR2) MANE Select ENSP00000496396.1:p.Gln25=
ENST00000434679.6:c.25+411G= (AVPR2) ENSP00000393397.1:n.25+411G=
ENST00000642393.1:c.97+3489C=
ENST00000646191.1:c.97+3489C=
ENST00000646375.1:c.75G= (AVPR2) ENSP00000496396.1:p.Gln25=
ENST00000337474.5:c.75G= (AVPR2) ENSP00000338072.5:p.Gln25=
ENST00000358927.6:c.75G= (AVPR2) ENSP00000351805.2:p.Gln25=
ENST00000370049.1:c.75G= (AVPR2) ENSP00000359066.1:p.Gln25=
ENST00000430697.1:c.75G= (AVPR2) ENSP00000393513.1:p.Gln25=
ENST00000434679.5:c.25+411G= (AVPR2) ENSP00000393397.1:n.25+411G=
ENST00000464967.5:n.154+3489C= (L1CAM)
NM_000054.4:c.75G= (AVPR2) NP_000045.1:p.Gln25=
NM_001146151.1:c.75G= (AVPR2) NP_001139623.1:p.Gln25=
NR_027419.1:n.559+411G= (AVPR2)
XM_006724828.2:c.75G= (AVPR2) XP_006724891.1:p.Gln25=
NM_000054.5:c.75G= (AVPR2) NP_000045.1:p.Gln25=
NM_001146151.2:c.75G= (AVPR2) NP_001139623.1:p.Gln25=
XM_006724828.3:c.75G= (AVPR2) XP_006724891.1:p.Gln25=
NM_000054.6:c.75G= (AVPR2) NP_000045.1:p.Gln25=
NM_001146151.3:c.75G= (AVPR2) NP_001139623.1:p.Gln25=
NR_027419.2:n.465+411G= (AVPR2)
NM_000054.7:c.75G= (AVPR2) MANE Select NP_000045.1:p.Gln25=