Canonical Allele Identifier: CA519666539

Linked Data

MyVariant Identifiers: chrX:g.153171797C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.153906343C>A , CM000685.2:g.153906343C>A GRCh38
NC_000023.10:g.153171797C>A , CM000685.1:g.153171797C>A GRCh37
NC_000023.9:g.152824991C>A NCBI36
NG_008687.1:g.6370C>A
NG_009645.3:g.7881G>T
NG_013220.1:g.24918G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000646375.2:c.837C>A (AVPR2) MANE Select ENSP00000496396.1:p.Val279=
ENST00000434679.6:c.*203C>A (AVPR2) ENSP00000393397.1:n.*203C>A
ENST00000642393.1:c.97+2727G>T
ENST00000646191.1:c.97+2727G>T
ENST00000646375.1:c.837C>A (AVPR2) ENSP00000496396.1:p.Val279=
ENST00000337474.5:c.837C>A (AVPR2) ENSP00000338072.5:p.Val279=
ENST00000358927.6:c.837C>A (AVPR2) ENSP00000351805.2:p.Val279=
ENST00000370049.1:c.837C>A (AVPR2) ENSP00000359066.1:p.Val279=
ENST00000430697.1:c.822+15C>A (AVPR2) ENSP00000393513.1:n.822+15C>A
ENST00000434679.5:c.*203C>A (AVPR2) ENSP00000393397.1:n.*203C>A
ENST00000464967.5:n.154+2727G>T (L1CAM)
NM_000054.4:c.837C>A (AVPR2) NP_000045.1:p.Val279=
NM_001146151.1:c.837C>A (AVPR2) NP_001139623.1:p.Val279=
NR_027419.1:n.884C>A (AVPR2)
XM_006724828.2:c.837C>A (AVPR2) XP_006724891.1:p.Val279=
NM_000054.5:c.837C>A (AVPR2) NP_000045.1:p.Val279=
NM_001146151.2:c.837C>A (AVPR2) NP_001139623.1:p.Val279=
XM_006724828.3:c.837C>A (AVPR2) XP_006724891.1:p.Val279=
NM_000054.6:c.837C>A (AVPR2) NP_000045.1:p.Val279=
NM_001146151.3:c.837C>A (AVPR2) NP_001139623.1:p.Val279=
NR_027419.2:n.790C>A (AVPR2)
NM_000054.7:c.837C>A (AVPR2) MANE Select NP_000045.1:p.Val279=