Canonical Allele Identifier: CA2473134703

Linked Data

ClinVar Variation Id: 2737429
ClinVar RCV Id: RCV003560309

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906269del , CM000685.2:g.153906269del GRCh38
NC_000023.10:g.153171723del , CM000685.1:g.153171723del GRCh37
NC_000023.9:g.152824917del NCBI36
NG_008687.1:g.6296del
NG_009645.3:g.7955del
NG_013220.1:g.24992del

Transcript Alleles

HGVS Amino-acid change
ENST00000646375.2:c.763del (AVPR2) MANE Select ENSP00000496396.1:p.Ser255AlafsTer16
ENST00000434679.6:c.*129del (AVPR2) ENSP00000393397.1:n.*129del
ENST00000642393.1:c.97+2801del
ENST00000646191.1:c.97+2801del
ENST00000646375.1:c.763del (AVPR2) ENSP00000496396.1:p.Ser255AlafsTer16
ENST00000337474.5:c.763del (AVPR2) ENSP00000338072.5:p.Ser255AlafsTer16
ENST00000358927.6:c.763del (AVPR2) ENSP00000351805.2:p.Ser255AlafsTer16
ENST00000370049.1:c.763del (AVPR2) ENSP00000359066.1:p.Ser255AlafsTer16
ENST00000430697.1:c.763del (AVPR2) ENSP00000393513.1:p.Ser255AlafsTer16
ENST00000434679.5:c.*129del (AVPR2) ENSP00000393397.1:n.*129del
ENST00000464967.5:n.154+2801del (L1CAM)
NM_000054.4:c.763del (AVPR2) NP_000045.1:p.Ser255AlafsTer16
NM_001146151.1:c.763del (AVPR2) NP_001139623.1:p.Ser255AlafsTer16
NR_027419.1:n.810del (AVPR2)
XM_006724828.2:c.763del (AVPR2) XP_006724891.1:p.Ser255AlafsTer16
NM_000054.5:c.763del (AVPR2) NP_000045.1:p.Ser255AlafsTer16
NM_001146151.2:c.763del (AVPR2) NP_001139623.1:p.Ser255AlafsTer16
XM_006724828.3:c.763del (AVPR2) XP_006724891.1:p.Ser255AlafsTer16
NM_000054.6:c.763del (AVPR2) NP_000045.1:p.Ser255AlafsTer16
NM_001146151.3:c.763del (AVPR2) NP_001139623.1:p.Ser255AlafsTer16
NR_027419.2:n.716del (AVPR2)
NM_000054.7:c.763del (AVPR2) MANE Select NP_000045.1:p.Ser255AlafsTer16