Canonical Allele Identifier: CA10555149

Gene: AVPR2 L1CAM

Linked Data

• dbSNP Id: rs782459549
• ExAC: X:153172231 C / T
• gnomAD v2: X-153172231-C-T
• gnomAD v3: X-153906777-C-T
• gnomAD v4: X-153906777-C-T
• MyVariant Identifiers: chrX:g.153172231C>T (hg19) ; chrX:g.153906777C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906777C>T , CM000685.2:g.153906777C>T	GRCh38
NC_000023.10:g.153172231C>T , CM000685.1:g.153172231C>T	GRCh37
NC_000023.9:g.152825425C>T	NCBI36
NG_008687.1:g.6804C>T
NG_009645.3:g.7447G>A
NG_013220.1:g.24484G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.*49C>T (AVPR2) MANE Select	ENSP00000496396.1:n.*49C>T
ENST00000434679.6:c.*531C>T (AVPR2)	ENSP00000393397.1:n.*531C>T
ENST00000642393.1:c.97+2293G>A
ENST00000646191.1:c.97+2293G>A
ENST00000646375.1:c.*49C>T (AVPR2)	ENSP00000496396.1:n.*49C>T
ENST00000337474.5:c.*49C>T (AVPR2)	ENSP00000338072.5:n.*49C>T
ENST00000358927.6:c.*49C>T (AVPR2)	ENSP00000351805.2:n.*49C>T
ENST00000370049.1:c.*341C>T (AVPR2)	ENSP00000359066.1:n.*341C>T
ENST00000430697.1:c.1077C>T (AVPR2)	ENSP00000393513.1:p.Ala359=
ENST00000434679.5:c.*531C>T (AVPR2)	ENSP00000393397.1:n.*531C>T
ENST00000464967.5:n.154+2293G>A (L1CAM)
NM_000054.4:c.*49C>T (AVPR2)	NP_000045.1:n.*49C>T
NM_001146151.1:c.*341C>T (AVPR2)	NP_001139623.1:n.*341C>T
NR_027419.1:n.1212C>T (AVPR2)
XM_006724828.2:c.*49C>T (AVPR2)	XP_006724891.1:n.*49C>T
NM_000054.5:c.*49C>T (AVPR2)	NP_000045.1:n.*49C>T
NM_001146151.2:c.*341C>T (AVPR2)	NP_001139623.1:n.*341C>T
XM_006724828.3:c.*49C>T (AVPR2)	XP_006724891.1:n.*49C>T
NM_000054.6:c.*49C>T (AVPR2)	NP_000045.1:n.*49C>T
NM_001146151.3:c.*341C>T (AVPR2)	NP_001139623.1:n.*341C>T
NR_027419.2:n.1118C>T (AVPR2)
NM_000054.7:c.*49C>T (AVPR2) MANE Select	NP_000045.1:n.*49C>T