Canonical Allele Identifier: CA10555089

Gene: AVPR2 L1CAM

Linked Data

• ClinVar Variation Id: 2717549
• ClinVar RCV Id: RCV003548832
• dbSNP Id: rs374156824
• ExAC: X:153171854 G / A
• gnomAD v2: X-153171854-G-A
• gnomAD v3: X-153906400-G-A
• gnomAD v4: X-153906400-G-A
• MyVariant Identifiers: chrX:g.153171854G>A (hg19) ; chrX:g.153906400G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906400G>A , CM000685.2:g.153906400G>A	GRCh38
NC_000023.10:g.153171854G>A , CM000685.1:g.153171854G>A	GRCh37
NC_000023.9:g.152825048G>A	NCBI36
NG_008687.1:g.6427G>A
NG_009645.3:g.7824C>T
NG_013220.1:g.24861C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.894G>A (AVPR2) MANE Select	ENSP00000496396.1:p.Pro298=
ENST00000434679.6:c.*260G>A (AVPR2)	ENSP00000393397.1:n.*260G>A
ENST00000642393.1:c.97+2670C>T
ENST00000646191.1:c.97+2670C>T
ENST00000646375.1:c.894G>A (AVPR2)	ENSP00000496396.1:p.Pro298=
ENST00000337474.5:c.894G>A (AVPR2)	ENSP00000338072.5:p.Pro298=
ENST00000358927.6:c.894G>A (AVPR2)	ENSP00000351805.2:p.Pro298=
ENST00000370049.1:c.894G>A (AVPR2)	ENSP00000359066.1:p.Pro298=
ENST00000430697.1:c.822+72G>A (AVPR2)	ENSP00000393513.1:n.822+72G>A
ENST00000434679.5:c.*260G>A (AVPR2)	ENSP00000393397.1:n.*260G>A
ENST00000464967.5:n.154+2670C>T (L1CAM)
NM_000054.4:c.894G>A (AVPR2)	NP_000045.1:p.Pro298=
NM_001146151.1:c.894G>A (AVPR2)	NP_001139623.1:p.Pro298=
NR_027419.1:n.941G>A (AVPR2)
XM_006724828.2:c.894G>A (AVPR2)	XP_006724891.1:p.Pro298=
NM_000054.5:c.894G>A (AVPR2)	NP_000045.1:p.Pro298=
NM_001146151.2:c.894G>A (AVPR2)	NP_001139623.1:p.Pro298=
XM_006724828.3:c.894G>A (AVPR2)	XP_006724891.1:p.Pro298=
NM_000054.6:c.894G>A (AVPR2)	NP_000045.1:p.Pro298=
NM_001146151.3:c.894G>A (AVPR2)	NP_001139623.1:p.Pro298=
NR_027419.2:n.847G>A (AVPR2)
NM_000054.7:c.894G>A (AVPR2) MANE Select	NP_000045.1:p.Pro298=