Canonical Allele Identifier: CA2466520844

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906621C= , CM000685.2:g.153906621C=	GRCh38
NC_000023.10:g.153172075C= , CM000685.1:g.153172075C=	GRCh37
NC_000023.9:g.152825269C=	NCBI36
NG_008687.1:g.6648C=
NG_009645.3:g.7603G=
NG_013220.1:g.24640G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000646375.2:c.1009C= (AVPR2) MANE Select	ENSP00000496396.1:p.Arg337=
ENST00000434679.6:c.*375C= (AVPR2)	ENSP00000393397.1:n.*375C=
ENST00000642393.1:c.97+2449G=
ENST00000646191.1:c.97+2449G=
ENST00000646375.1:c.1009C= (AVPR2)	ENSP00000496396.1:p.Arg337=
ENST00000337474.5:c.1009C= (AVPR2)	ENSP00000338072.5:p.Arg337=
ENST00000358927.6:c.1009C= (AVPR2)	ENSP00000351805.2:p.Arg337=
ENST00000370049.1:c.*185C= (AVPR2)	ENSP00000359066.1:n.*185C=
ENST00000430697.1:c.921C= (AVPR2)	ENSP00000393513.1:p.Cys307=
ENST00000434679.5:c.*375C= (AVPR2)	ENSP00000393397.1:n.*375C=
ENST00000464967.5:n.154+2449G= (L1CAM)
NM_000054.4:c.1009C= (AVPR2)	NP_000045.1:p.Arg337=
NM_001146151.1:c.*185C= (AVPR2)	NP_001139623.1:n.*185C=
NR_027419.1:n.1056C= (AVPR2)
XM_006724828.2:c.1009C= (AVPR2)	XP_006724891.1:p.Arg337=
NM_000054.5:c.1009C= (AVPR2)	NP_000045.1:p.Arg337=
NM_001146151.2:c.*185C= (AVPR2)	NP_001139623.1:n.*185C=
XM_006724828.3:c.1009C= (AVPR2)	XP_006724891.1:p.Arg337=
NM_000054.6:c.1009C= (AVPR2)	NP_000045.1:p.Arg337=
NM_001146151.3:c.*185C= (AVPR2)	NP_001139623.1:n.*185C=
NR_027419.2:n.962C= (AVPR2)
NM_000054.7:c.1009C= (AVPR2) MANE Select	NP_000045.1:p.Arg337=