Canonical Allele Identifier: CA2466520896

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906739G= , CM000685.2:g.153906739G=	GRCh38
NC_000023.10:g.153172193G= , CM000685.1:g.153172193G=	GRCh37
NC_000023.9:g.152825387G=	NCBI36
NG_008687.1:g.6766G=
NG_009645.3:g.7485C=
NG_013220.1:g.24522C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.*11G= (AVPR2) MANE Select	ENSP00000496396.1:n.*11G=
ENST00000434679.6:c.*493G= (AVPR2)	ENSP00000393397.1:n.*493G=
ENST00000642393.1:c.97+2331C=
ENST00000646191.1:c.97+2331C=
ENST00000646375.1:c.*11G= (AVPR2)	ENSP00000496396.1:n.*11G=
ENST00000337474.5:c.*11G= (AVPR2)	ENSP00000338072.5:n.*11G=
ENST00000358927.6:c.*11G= (AVPR2)	ENSP00000351805.2:n.*11G=
ENST00000370049.1:c.*303G= (AVPR2)	ENSP00000359066.1:n.*303G=
ENST00000430697.1:c.1039G= (AVPR2)	ENSP00000393513.1:p.Gly347=
ENST00000434679.5:c.*493G= (AVPR2)	ENSP00000393397.1:n.*493G=
ENST00000464967.5:n.154+2331C= (L1CAM)
NM_000054.4:c.*11G= (AVPR2)	NP_000045.1:n.*11G=
NM_001146151.1:c.*303G= (AVPR2)	NP_001139623.1:n.*303G=
NR_027419.1:n.1174G= (AVPR2)
XM_006724828.2:c.*11G= (AVPR2)	XP_006724891.1:n.*11G=
NM_000054.5:c.*11G= (AVPR2)	NP_000045.1:n.*11G=
NM_001146151.2:c.*303G= (AVPR2)	NP_001139623.1:n.*303G=
XM_006724828.3:c.*11G= (AVPR2)	XP_006724891.1:n.*11G=
NM_000054.6:c.*11G= (AVPR2)	NP_000045.1:n.*11G=
NM_001146151.3:c.*303G= (AVPR2)	NP_001139623.1:n.*303G=
NR_027419.2:n.1080G= (AVPR2)
NM_000054.7:c.*11G= (AVPR2) MANE Select	NP_000045.1:n.*11G=