Canonical Allele Identifier: CA645158877

Gene: AVPR2 L1CAM

Linked Data

• dbSNP Id: rs1330941142
• gnomAD v2: X-153172293-G-C
• gnomAD v4: X-153906839-G-C
• MyVariant Identifiers: chrX:g.153172293G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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