Canonical Allele Identifier: CA415107331

Gene: AVPR2 L1CAM

Linked Data

• gnomAD v4: X-153906087-C-T
• MyVariant Identifiers: chrX:g.153171541C>T (hg19) ; chrX:g.153906087C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906087C>T , CM000685.2:g.153906087C>T	GRCh38
NC_000023.10:g.153171541C>T , CM000685.1:g.153171541C>T	GRCh37
NC_000023.9:g.152824735C>T	NCBI36
NG_008687.1:g.6114C>T
NG_009645.3:g.8137G>A
NG_013220.1:g.25174G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.581C>T (AVPR2) MANE Select	ENSP00000496396.1:p.Ala194Val
ENST00000434679.6:c.94C>T (AVPR2)	ENSP00000393397.1:p.Pro32Ser
ENST00000642393.1:c.97+2983G>A
ENST00000646191.1:c.97+2983G>A
ENST00000646375.1:c.581C>T (AVPR2)	ENSP00000496396.1:p.Ala194Val
ENST00000337474.5:c.581C>T (AVPR2)	ENSP00000338072.5:p.Ala194Val
ENST00000358927.6:c.581C>T (AVPR2)	ENSP00000351805.2:p.Ala194Val
ENST00000370049.1:c.581C>T (AVPR2)	ENSP00000359066.1:p.Ala194Val
ENST00000430697.1:c.581C>T (AVPR2)	ENSP00000393513.1:p.Ala194Val
ENST00000434679.5:c.94C>T (AVPR2)	ENSP00000393397.1:p.Pro32Ser
ENST00000464967.5:n.154+2983G>A (L1CAM)
NM_000054.4:c.581C>T (AVPR2)	NP_000045.1:p.Ala194Val
NM_001146151.1:c.581C>T (AVPR2)	NP_001139623.1:p.Ala194Val
NR_027419.1:n.628C>T (AVPR2)
XM_006724828.2:c.581C>T (AVPR2)	XP_006724891.1:p.Ala194Val
NM_000054.5:c.581C>T (AVPR2)	NP_000045.1:p.Ala194Val
NM_001146151.2:c.581C>T (AVPR2)	NP_001139623.1:p.Ala194Val
XM_006724828.3:c.581C>T (AVPR2)	XP_006724891.1:p.Ala194Val
NM_000054.6:c.581C>T (AVPR2)	NP_000045.1:p.Ala194Val
NM_001146151.3:c.581C>T (AVPR2)	NP_001139623.1:p.Ala194Val
NR_027419.2:n.534C>T (AVPR2)
NM_000054.7:c.581C>T (AVPR2) MANE Select	NP_000045.1:p.Ala194Val