Canonical Allele Identifier: CA873286562

Linked Data

dbSNP Id: rs1195901521
MyVariant Identifiers: chrX:g.153906813G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906813G>A , CM000685.2:g.153906813G>A GRCh38
NC_000023.10:g.153172267G>A , CM000685.1:g.153172267G>A GRCh37
NC_000023.9:g.152825461G>A NCBI36
NG_008687.1:g.6840G>A
NG_009645.3:g.7411C>T
NG_013220.1:g.24448C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.*85G>A (AVPR2) MANE Select ENSP00000496396.1:n.*85G>A
ENST00000434679.6:c.*567G>A (AVPR2) ENSP00000393397.1:n.*567G>A
ENST00000642393.1:c.97+2257C>T
ENST00000646191.1:c.97+2257C>T
ENST00000646375.1:c.*85G>A (AVPR2) ENSP00000496396.1:n.*85G>A
ENST00000337474.5:c.*85G>A (AVPR2) ENSP00000338072.5:n.*85G>A
ENST00000358927.6:c.*85G>A (AVPR2) ENSP00000351805.2:n.*85G>A
ENST00000430697.1:c.1113G>A (AVPR2) ENSP00000393513.1:p.Gly371=
ENST00000434679.5:c.*567G>A (AVPR2) ENSP00000393397.1:n.*567G>A
ENST00000464967.5:n.154+2257C>T (L1CAM)
NM_000054.4:c.*85G>A (AVPR2) NP_000045.1:n.*85G>A
NM_001146151.1:c.*377G>A (AVPR2) NP_001139623.1:n.*377G>A
NR_027419.1:n.1248G>A (AVPR2)
XM_006724828.2:c.*85G>A (AVPR2) XP_006724891.1:n.*85G>A
NM_000054.5:c.*85G>A (AVPR2) NP_000045.1:n.*85G>A
NM_001146151.2:c.*377G>A (AVPR2) NP_001139623.1:n.*377G>A
XM_006724828.3:c.*85G>A (AVPR2) XP_006724891.1:n.*85G>A
NM_000054.6:c.*85G>A (AVPR2) NP_000045.1:n.*85G>A
NM_001146151.3:c.*377G>A (AVPR2) NP_001139623.1:n.*377G>A
NR_027419.2:n.1154G>A (AVPR2)
NM_000054.7:c.*85G>A (AVPR2) MANE Select NP_000045.1:n.*85G>A