Canonical Allele Identifier: CA2466520765

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906360C= , CM000685.2:g.153906360C=	GRCh38
NC_000023.10:g.153171814C= , CM000685.1:g.153171814C=	GRCh37
NC_000023.9:g.152825008C=	NCBI36
NG_008687.1:g.6387C=
NG_009645.3:g.7864G=
NG_013220.1:g.24901G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.854C= (AVPR2) MANE Select	ENSP00000496396.1:p.Ala285=
ENST00000434679.6:c.*220C= (AVPR2)	ENSP00000393397.1:n.*220C=
ENST00000642393.1:c.97+2710G=
ENST00000646191.1:c.97+2710G=
ENST00000646375.1:c.854C= (AVPR2)	ENSP00000496396.1:p.Ala285=
ENST00000337474.5:c.854C= (AVPR2)	ENSP00000338072.5:p.Ala285=
ENST00000358927.6:c.854C= (AVPR2)	ENSP00000351805.2:p.Ala285=
ENST00000370049.1:c.854C= (AVPR2)	ENSP00000359066.1:p.Ala285=
ENST00000430697.1:c.822+32C= (AVPR2)	ENSP00000393513.1:n.822+32C=
ENST00000434679.5:c.*220C= (AVPR2)	ENSP00000393397.1:n.*220C=
ENST00000464967.5:n.154+2710G= (L1CAM)
NM_000054.4:c.854C= (AVPR2)	NP_000045.1:p.Ala285=
NM_001146151.1:c.854C= (AVPR2)	NP_001139623.1:p.Ala285=
NR_027419.1:n.901C= (AVPR2)
XM_006724828.2:c.854C= (AVPR2)	XP_006724891.1:p.Ala285=
NM_000054.5:c.854C= (AVPR2)	NP_000045.1:p.Ala285=
NM_001146151.2:c.854C= (AVPR2)	NP_001139623.1:p.Ala285=
XM_006724828.3:c.854C= (AVPR2)	XP_006724891.1:p.Ala285=
NM_000054.6:c.854C= (AVPR2)	NP_000045.1:p.Ala285=
NM_001146151.3:c.854C= (AVPR2)	NP_001139623.1:p.Ala285=
NR_027419.2:n.807C= (AVPR2)
NM_000054.7:c.854C= (AVPR2) MANE Select	NP_000045.1:p.Ala285=