Canonical Allele Identifier: CA873286572

Gene: AVPR2 L1CAM

Linked Data

• dbSNP Id: rs1330941142
• gnomAD v4: X-153906839-G-A
• MyVariant Identifiers: chrX:g.153906839G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906839G>A , CM000685.2:g.153906839G>A	GRCh38
NC_000023.10:g.153172293G>A , CM000685.1:g.153172293G>A	GRCh37
NC_000023.9:g.152825487G>A	NCBI36
NG_008687.1:g.6866G>A
NG_009645.3:g.7385C>T
NG_013220.1:g.24422C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.*111G>A (AVPR2) MANE Select	ENSP00000496396.1:n.*111G>A
ENST00000434679.6:c.*593G>A (AVPR2)	ENSP00000393397.1:n.*593G>A
ENST00000642393.1:c.97+2231C>T
ENST00000646191.1:c.97+2231C>T
ENST00000646375.1:c.*111G>A (AVPR2)	ENSP00000496396.1:n.*111G>A
ENST00000337474.5:c.*111G>A (AVPR2)	ENSP00000338072.5:n.*111G>A
ENST00000358927.6:c.*111G>A (AVPR2)	ENSP00000351805.2:n.*111G>A
ENST00000434679.5:c.*593G>A (AVPR2)	ENSP00000393397.1:n.*593G>A
ENST00000464967.5:n.154+2231C>T (L1CAM)
NM_000054.4:c.*111G>A (AVPR2)	NP_000045.1:n.*111G>A
NM_001146151.1:c.*403G>A (AVPR2)	NP_001139623.1:n.*403G>A
NR_027419.1:n.1274G>A (AVPR2)
XM_006724828.2:c.*111G>A (AVPR2)	XP_006724891.1:n.*111G>A
NM_000054.5:c.*111G>A (AVPR2)	NP_000045.1:n.*111G>A
NM_001146151.2:c.*403G>A (AVPR2)	NP_001139623.1:n.*403G>A
XM_006724828.3:c.*111G>A (AVPR2)	XP_006724891.1:n.*111G>A
NM_000054.6:c.*111G>A (AVPR2)	NP_000045.1:n.*111G>A
NM_001146151.3:c.*403G>A (AVPR2)	NP_001139623.1:n.*403G>A
NR_027419.2:n.1180G>A (AVPR2)
NM_000054.7:c.*111G>A (AVPR2) MANE Select	NP_000045.1:n.*111G>A