Canonical Allele Identifier: CA415110445

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906521A>C , CM000685.2:g.153906521A>C GRCh38
NC_000023.10:g.153171975A>C , CM000685.1:g.153171975A>C GRCh37
NC_000023.9:g.152825169A>C NCBI36
NG_008687.1:g.6548A>C
NG_009645.3:g.7703T>G
NG_013220.1:g.24740T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.911-2A>C (AVPR2) MANE Select ENSP00000496396.1:n.911-2A>C
ENST00000434679.6:c.*277-2A>C (AVPR2) ENSP00000393397.1:n.*277-2A>C
ENST00000642393.1:c.97+2549T>G
ENST00000646191.1:c.97+2549T>G
ENST00000646375.1:c.911-2A>C (AVPR2) ENSP00000496396.1:n.911-2A>C
ENST00000337474.5:c.911-2A>C (AVPR2) ENSP00000338072.5:n.911-2A>C
ENST00000358927.6:c.911-2A>C (AVPR2) ENSP00000351805.2:n.911-2A>C
ENST00000370049.1:c.*85A>C (AVPR2) ENSP00000359066.1:n.*85A>C
ENST00000430697.1:c.823-2A>C (AVPR2) ENSP00000393513.1:n.823-2A>C
ENST00000434679.5:c.*277-2A>C (AVPR2) ENSP00000393397.1:n.*277-2A>C
ENST00000464967.5:n.154+2549T>G (L1CAM)
NM_000054.4:c.911-2A>C (AVPR2) NP_000045.1:n.911-2A>C
NM_001146151.1:c.*85A>C (AVPR2) NP_001139623.1:n.*85A>C
NR_027419.1:n.958-2A>C (AVPR2)
XM_006724828.2:c.911-2A>C (AVPR2) XP_006724891.1:n.911-2A>C
NM_000054.5:c.911-2A>C (AVPR2) NP_000045.1:n.911-2A>C
NM_001146151.2:c.*85A>C (AVPR2) NP_001139623.1:n.*85A>C
XM_006724828.3:c.911-2A>C (AVPR2) XP_006724891.1:n.911-2A>C
NM_000054.6:c.911-2A>C (AVPR2) NP_000045.1:n.911-2A>C
NM_001146151.3:c.*85A>C (AVPR2) NP_001139623.1:n.*85A>C
NR_027419.2:n.864-2A>C (AVPR2)
NM_000054.7:c.911-2A>C (AVPR2) MANE Select NP_000045.1:n.911-2A>C