Canonical Allele Identifier: CA415109213

Gene: AVPR2 L1CAM

Linked Data

• ClinVar Variation Id: 804119
• ClinVar RCV Id: RCV000990992
• dbSNP Id: rs1557100878
• gnomAD v2: X-153171744-G-A
• gnomAD v4: X-153906290-G-A
• MyVariant Identifiers: chrX:g.153171744G>A (hg19) ; chrX:g.153906290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906290G>A , CM000685.2:g.153906290G>A	GRCh38
NC_000023.10:g.153171744G>A , CM000685.1:g.153171744G>A	GRCh37
NC_000023.9:g.152824938G>A	NCBI36
NG_008687.1:g.6317G>A
NG_009645.3:g.7934C>T
NG_013220.1:g.24971C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646375.2:c.784G>A (AVPR2) MANE Select	ENSP00000496396.1:p.Val262Met
ENST00000434679.6:c.*150G>A (AVPR2)	ENSP00000393397.1:n.*150G>A
ENST00000642393.1:c.97+2780C>T
ENST00000646191.1:c.97+2780C>T
ENST00000646375.1:c.784G>A (AVPR2)	ENSP00000496396.1:p.Val262Met
ENST00000337474.5:c.784G>A (AVPR2)	ENSP00000338072.5:p.Val262Met
ENST00000358927.6:c.784G>A (AVPR2)	ENSP00000351805.2:p.Val262Met
ENST00000370049.1:c.784G>A (AVPR2)	ENSP00000359066.1:p.Val262Met
ENST00000430697.1:c.784G>A (AVPR2)	ENSP00000393513.1:p.Val262Met
ENST00000434679.5:c.*150G>A (AVPR2)	ENSP00000393397.1:n.*150G>A
ENST00000464967.5:n.154+2780C>T (L1CAM)
NM_000054.4:c.784G>A (AVPR2)	NP_000045.1:p.Val262Met
NM_001146151.1:c.784G>A (AVPR2)	NP_001139623.1:p.Val262Met
NR_027419.1:n.831G>A (AVPR2)
XM_006724828.2:c.784G>A (AVPR2)	XP_006724891.1:p.Val262Met
NM_000054.5:c.784G>A (AVPR2)	NP_000045.1:p.Val262Met
NM_001146151.2:c.784G>A (AVPR2)	NP_001139623.1:p.Val262Met
XM_006724828.3:c.784G>A (AVPR2)	XP_006724891.1:p.Val262Met
NM_000054.6:c.784G>A (AVPR2)	NP_000045.1:p.Val262Met
NM_001146151.3:c.784G>A (AVPR2)	NP_001139623.1:p.Val262Met
NR_027419.2:n.737G>A (AVPR2)
NM_000054.7:c.784G>A (AVPR2) MANE Select	NP_000045.1:p.Val262Met