Canonical Allele Identifier: CA415110461

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906522G>C , CM000685.2:g.153906522G>C GRCh38
NC_000023.10:g.153171976G>C , CM000685.1:g.153171976G>C GRCh37
NC_000023.9:g.152825170G>C NCBI36
NG_008687.1:g.6549G>C
NG_009645.3:g.7702C>G
NG_013220.1:g.24739C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.911-1G>C (AVPR2) MANE Select ENSP00000496396.1:n.911-1G>C
ENST00000434679.6:c.*277-1G>C (AVPR2) ENSP00000393397.1:n.*277-1G>C
ENST00000642393.1:c.97+2548C>G
ENST00000646191.1:c.97+2548C>G
ENST00000646375.1:c.911-1G>C (AVPR2) ENSP00000496396.1:n.911-1G>C
ENST00000337474.5:c.911-1G>C (AVPR2) ENSP00000338072.5:n.911-1G>C
ENST00000358927.6:c.911-1G>C (AVPR2) ENSP00000351805.2:n.911-1G>C
ENST00000370049.1:c.*86G>C (AVPR2) ENSP00000359066.1:n.*86G>C
ENST00000430697.1:c.823-1G>C (AVPR2) ENSP00000393513.1:n.823-1G>C
ENST00000434679.5:c.*277-1G>C (AVPR2) ENSP00000393397.1:n.*277-1G>C
ENST00000464967.5:n.154+2548C>G (L1CAM)
NM_000054.4:c.911-1G>C (AVPR2) NP_000045.1:n.911-1G>C
NM_001146151.1:c.*86G>C (AVPR2) NP_001139623.1:n.*86G>C
NR_027419.1:n.958-1G>C (AVPR2)
XM_006724828.2:c.911-1G>C (AVPR2) XP_006724891.1:n.911-1G>C
NM_000054.5:c.911-1G>C (AVPR2) NP_000045.1:n.911-1G>C
NM_001146151.2:c.*86G>C (AVPR2) NP_001139623.1:n.*86G>C
XM_006724828.3:c.911-1G>C (AVPR2) XP_006724891.1:n.911-1G>C
NM_000054.6:c.911-1G>C (AVPR2) NP_000045.1:n.911-1G>C
NM_001146151.3:c.*86G>C (AVPR2) NP_001139623.1:n.*86G>C
NR_027419.2:n.864-1G>C (AVPR2)
NM_000054.7:c.911-1G>C (AVPR2) MANE Select NP_000045.1:n.911-1G>C