Canonical Allele Identifier: CA2466520792

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906434T= , CM000685.2:g.153906434T=	GRCh38
NC_000023.10:g.153171888T= , CM000685.1:g.153171888T=	GRCh37
NC_000023.9:g.152825082T=	NCBI36
NG_008687.1:g.6461T=
NG_009645.3:g.7790A=
NG_013220.1:g.24827A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646375.2:c.910+18T= (AVPR2) MANE Select	ENSP00000496396.1:n.910+18T=
ENST00000434679.6:c.*276+18T= (AVPR2)	ENSP00000393397.1:n.*276+18T=
ENST00000642393.1:c.97+2636A=
ENST00000646191.1:c.97+2636A=
ENST00000646375.1:c.910+18T= (AVPR2)	ENSP00000496396.1:n.910+18T=
ENST00000337474.5:c.910+18T= (AVPR2)	ENSP00000338072.5:n.910+18T=
ENST00000358927.6:c.910+18T= (AVPR2)	ENSP00000351805.2:n.910+18T=
ENST00000370049.1:c.928T= (AVPR2)	ENSP00000359066.1:p.Ter310=
ENST00000430697.1:c.823-89T= (AVPR2)	ENSP00000393513.1:n.823-89T=
ENST00000434679.5:c.*276+18T= (AVPR2)	ENSP00000393397.1:n.*276+18T=
ENST00000464967.5:n.154+2636A= (L1CAM)
NM_000054.4:c.910+18T= (AVPR2)	NP_000045.1:n.910+18T=
NM_001146151.1:c.928T= (AVPR2)	NP_001139623.1:p.Ter310=
NR_027419.1:n.957+18T= (AVPR2)
XM_006724828.2:c.910+18T= (AVPR2)	XP_006724891.1:n.910+18T=
NM_000054.5:c.910+18T= (AVPR2)	NP_000045.1:n.910+18T=
NM_001146151.2:c.928T= (AVPR2)	NP_001139623.1:p.Ter310=
XM_006724828.3:c.910+18T= (AVPR2)	XP_006724891.1:n.910+18T=
NM_000054.6:c.910+18T= (AVPR2)	NP_000045.1:n.910+18T=
NM_001146151.3:c.928T= (AVPR2)	NP_001139623.1:p.Ter310=
NR_027419.2:n.863+18T= (AVPR2)
NM_000054.7:c.910+18T= (AVPR2) MANE Select	NP_000045.1:n.910+18T=