Canonical Allele Identifier: CA2695073593

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153905511del , CM000685.2:g.153905511del GRCh38
NC_000023.10:g.153170965del , CM000685.1:g.153170965del GRCh37
NC_000023.9:g.152824159del NCBI36
NG_008687.1:g.5538del
NG_009645.3:g.8715del
NG_013220.1:g.25752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.26-21del (AVPR2) MANE Select ENSP00000496396.1:n.26-21del
ENST00000434679.6:c.25+341del (AVPR2) ENSP00000393397.1:n.25+341del
ENST00000642393.1:c.97+3561del
ENST00000646191.1:c.97+3561del
ENST00000646375.1:c.26-21del (AVPR2) ENSP00000496396.1:n.26-21del
ENST00000337474.5:c.26-21del (AVPR2) ENSP00000338072.5:n.26-21del
ENST00000358927.6:c.26-21del (AVPR2) ENSP00000351805.2:n.26-21del
ENST00000370049.1:c.26-21del (AVPR2) ENSP00000359066.1:n.26-21del
ENST00000430697.1:c.26-21del (AVPR2) ENSP00000393513.1:n.26-21del
ENST00000434679.5:c.25+341del (AVPR2) ENSP00000393397.1:n.25+341del
ENST00000464967.5:n.154+3561del (L1CAM)
NM_000054.4:c.26-21del (AVPR2) NP_000045.1:n.26-21del
NM_001146151.1:c.26-21del (AVPR2) NP_001139623.1:n.26-21del
NR_027419.1:n.559+341del (AVPR2)
XM_006724828.2:c.26-21del (AVPR2) XP_006724891.1:n.26-21del
NM_000054.5:c.26-21del (AVPR2) NP_000045.1:n.26-21del
NM_001146151.2:c.26-21del (AVPR2) NP_001139623.1:n.26-21del
XM_006724828.3:c.26-21del (AVPR2) XP_006724891.1:n.26-21del
NM_000054.6:c.26-21del (AVPR2) NP_000045.1:n.26-21del
NM_001146151.3:c.26-21del (AVPR2) NP_001139623.1:n.26-21del
NR_027419.2:n.465+341del (AVPR2)
NM_000054.7:c.26-21del (AVPR2) MANE Select NP_000045.1:n.26-21del