Canonical Allele Identifier: CA519249329

Gene: AVPR2 L1CAM

Linked Data

• ClinVar Variation Id: 765037
• ClinVar RCV Id: RCV000943415
• dbSNP Id: rs1331353572
• gnomAD v2: X-153171066-C-T
• gnomAD v3: X-153905612-C-T
• gnomAD v4: X-153905612-C-T
• MyVariant Identifiers: chrX:g.153171066C>T (hg19) ; chrX:g.153905612C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153905612C>T , CM000685.2:g.153905612C>T	GRCh38
NC_000023.10:g.153171066C>T , CM000685.1:g.153171066C>T	GRCh37
NC_000023.9:g.152824260C>T	NCBI36
NG_008687.1:g.5639C>T
NG_009645.3:g.8612G>A
NG_013220.1:g.25649G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.106C>T (AVPR2) MANE Select	ENSP00000496396.1:p.Leu36=
ENST00000434679.6:c.26-407C>T (AVPR2)	ENSP00000393397.1:n.26-407C>T
ENST00000642393.1:c.97+3458G>A
ENST00000646191.1:c.97+3458G>A
ENST00000646375.1:c.106C>T (AVPR2)	ENSP00000496396.1:p.Leu36=
ENST00000337474.5:c.106C>T (AVPR2)	ENSP00000338072.5:p.Leu36=
ENST00000358927.6:c.106C>T (AVPR2)	ENSP00000351805.2:p.Leu36=
ENST00000370049.1:c.106C>T (AVPR2)	ENSP00000359066.1:p.Leu36=
ENST00000430697.1:c.106C>T (AVPR2)	ENSP00000393513.1:p.Leu36=
ENST00000434679.5:c.26-407C>T (AVPR2)	ENSP00000393397.1:n.26-407C>T
ENST00000464967.5:n.154+3458G>A (L1CAM)
NM_000054.4:c.106C>T (AVPR2)	NP_000045.1:p.Leu36=
NM_001146151.1:c.106C>T (AVPR2)	NP_001139623.1:p.Leu36=
NR_027419.1:n.560-407C>T (AVPR2)
XM_006724828.2:c.106C>T (AVPR2)	XP_006724891.1:p.Leu36=
NM_000054.5:c.106C>T (AVPR2)	NP_000045.1:p.Leu36=
NM_001146151.2:c.106C>T (AVPR2)	NP_001139623.1:p.Leu36=
XM_006724828.3:c.106C>T (AVPR2)	XP_006724891.1:p.Leu36=
NM_000054.6:c.106C>T (AVPR2)	NP_000045.1:p.Leu36=
NM_001146151.3:c.106C>T (AVPR2)	NP_001139623.1:p.Leu36=
NR_027419.2:n.466-407C>T (AVPR2)
NM_000054.7:c.106C>T (AVPR2) MANE Select	NP_000045.1:p.Leu36=