Canonical Allele Identifier: CA2466520675

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906181G= , CM000685.2:g.153906181G= GRCh38
NC_000023.10:g.153171635G= , CM000685.1:g.153171635G= GRCh37
NC_000023.9:g.152824829G= NCBI36
NG_008687.1:g.6208G=
NG_009645.3:g.8043C=
NG_013220.1:g.25080C=

Transcript Alleles

HGVS Amino-acid change
ENST00000646375.2:c.675G= (AVPR2) MANE Select ENSP00000496396.1:p.Gln225=
ENST00000434679.6:c.*41G= (AVPR2) ENSP00000393397.1:n.*41G=
ENST00000642393.1:c.97+2889C=
ENST00000646191.1:c.97+2889C=
ENST00000646375.1:c.675G= (AVPR2) ENSP00000496396.1:p.Gln225=
ENST00000337474.5:c.675G= (AVPR2) ENSP00000338072.5:p.Gln225=
ENST00000358927.6:c.675G= (AVPR2) ENSP00000351805.2:p.Gln225=
ENST00000370049.1:c.675G= (AVPR2) ENSP00000359066.1:p.Gln225=
ENST00000430697.1:c.675G= (AVPR2) ENSP00000393513.1:p.Gln225=
ENST00000434679.5:c.*41G= (AVPR2) ENSP00000393397.1:n.*41G=
ENST00000464967.5:n.154+2889C= (L1CAM)
NM_000054.4:c.675G= (AVPR2) NP_000045.1:p.Gln225=
NM_001146151.1:c.675G= (AVPR2) NP_001139623.1:p.Gln225=
NR_027419.1:n.722G= (AVPR2)
XM_006724828.2:c.675G= (AVPR2) XP_006724891.1:p.Gln225=
NM_000054.5:c.675G= (AVPR2) NP_000045.1:p.Gln225=
NM_001146151.2:c.675G= (AVPR2) NP_001139623.1:p.Gln225=
XM_006724828.3:c.675G= (AVPR2) XP_006724891.1:p.Gln225=
NM_000054.6:c.675G= (AVPR2) NP_000045.1:p.Gln225=
NM_001146151.3:c.675G= (AVPR2) NP_001139623.1:p.Gln225=
NR_027419.2:n.628G= (AVPR2)
NM_000054.7:c.675G= (AVPR2) MANE Select NP_000045.1:p.Gln225=