Canonical Allele Identifier: CA2695236921

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153905825_153905842del , CM000685.2:g.153905825_153905842del GRCh38
NC_000023.10:g.153171279_153171296del , CM000685.1:g.153171279_153171296del GRCh37
NC_000023.9:g.152824473_152824490del NCBI36
NG_008687.1:g.5852_5869del
NG_009645.3:g.8384_8401del
NG_013220.1:g.25421_25438del

Transcript Alleles

HGVS Amino-acid change
ENST00000646375.2:c.319_336del (AVPR2) MANE Select ENSP00000496396.1:p.Gly107_Cys112del
ENST00000434679.6:c.26-194_26-177del (AVPR2) ENSP00000393397.1:n.26-194_26-177del
ENST00000642393.1:c.97+3230_97+3247del
ENST00000646191.1:c.97+3230_97+3247del
ENST00000646375.1:c.319_336del (AVPR2) ENSP00000496396.1:p.Gly107_Cys112del
ENST00000337474.5:c.319_336del (AVPR2) ENSP00000338072.5:p.Gly107_Cys112del
ENST00000358927.6:c.319_336del (AVPR2) ENSP00000351805.2:p.Gly107_Cys112del
ENST00000370049.1:c.319_336del (AVPR2) ENSP00000359066.1:p.Gly107_Cys112del
ENST00000430697.1:c.319_336del (AVPR2) ENSP00000393513.1:p.Gly107_Cys112del
ENST00000434679.5:c.26-194_26-177del (AVPR2) ENSP00000393397.1:n.26-194_26-177del
ENST00000464967.5:n.154+3230_154+3247del (L1CAM)
NM_000054.4:c.319_336del (AVPR2) NP_000045.1:p.Gly107_Cys112del
NM_001146151.1:c.319_336del (AVPR2) NP_001139623.1:p.Gly107_Cys112del
NR_027419.1:n.560-194_560-177del (AVPR2)
XM_006724828.2:c.319_336del (AVPR2) XP_006724891.1:p.Gly107_Cys112del
NM_000054.5:c.319_336del (AVPR2) NP_000045.1:p.Gly107_Cys112del
NM_001146151.2:c.319_336del (AVPR2) NP_001139623.1:p.Gly107_Cys112del
XM_006724828.3:c.319_336del (AVPR2) XP_006724891.1:p.Gly107_Cys112del
NM_000054.6:c.319_336del (AVPR2) NP_000045.1:p.Gly107_Cys112del
NM_001146151.3:c.319_336del (AVPR2) NP_001139623.1:p.Gly107_Cys112del
NR_027419.2:n.466-194_466-177del (AVPR2)
NM_000054.7:c.319_336del (AVPR2) MANE Select NP_000045.1:p.Gly107_Cys112del