Canonical Allele Identifier: CA415112442

Gene: AVPR2 L1CAM

Linked Data

• MyVariant Identifiers: chrX:g.153172209A>T (hg19) ; chrX:g.153906755A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906755A>T , CM000685.2:g.153906755A>T	GRCh38
NC_000023.10:g.153172209A>T , CM000685.1:g.153172209A>T	GRCh37
NC_000023.9:g.152825403A>T	NCBI36
NG_008687.1:g.6782A>T
NG_009645.3:g.7469T>A
NG_013220.1:g.24506T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.*27A>T (AVPR2) MANE Select	ENSP00000496396.1:n.*27A>T
ENST00000434679.6:c.*509A>T (AVPR2)	ENSP00000393397.1:n.*509A>T
ENST00000642393.1:c.97+2315T>A
ENST00000646191.1:c.97+2315T>A
ENST00000646375.1:c.*27A>T (AVPR2)	ENSP00000496396.1:n.*27A>T
ENST00000337474.5:c.*27A>T (AVPR2)	ENSP00000338072.5:n.*27A>T
ENST00000358927.6:c.*27A>T (AVPR2)	ENSP00000351805.2:n.*27A>T
ENST00000370049.1:c.*319A>T (AVPR2)	ENSP00000359066.1:n.*319A>T
ENST00000430697.1:c.1055A>T (AVPR2)	ENSP00000393513.1:p.Glu352Val
ENST00000434679.5:c.*509A>T (AVPR2)	ENSP00000393397.1:n.*509A>T
ENST00000464967.5:n.154+2315T>A (L1CAM)
NM_000054.4:c.*27A>T (AVPR2)	NP_000045.1:n.*27A>T
NM_001146151.1:c.*319A>T (AVPR2)	NP_001139623.1:n.*319A>T
NR_027419.1:n.1190A>T (AVPR2)
XM_006724828.2:c.*27A>T (AVPR2)	XP_006724891.1:n.*27A>T
NM_000054.5:c.*27A>T (AVPR2)	NP_000045.1:n.*27A>T
NM_001146151.2:c.*319A>T (AVPR2)	NP_001139623.1:n.*319A>T
XM_006724828.3:c.*27A>T (AVPR2)	XP_006724891.1:n.*27A>T
NM_000054.6:c.*27A>T (AVPR2)	NP_000045.1:n.*27A>T
NM_001146151.3:c.*319A>T (AVPR2)	NP_001139623.1:n.*319A>T
NR_027419.2:n.1096A>T (AVPR2)
NM_000054.7:c.*27A>T (AVPR2) MANE Select	NP_000045.1:n.*27A>T