Canonical Allele Identifier: CA2466520931

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906826T= , CM000685.2:g.153906826T=	GRCh38
NC_000023.10:g.153172280T= , CM000685.1:g.153172280T=	GRCh37
NC_000023.9:g.152825474T=	NCBI36
NG_008687.1:g.6853T=
NG_009645.3:g.7398A=
NG_013220.1:g.24435A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.*98T= (AVPR2) MANE Select	ENSP00000496396.1:n.*98T=
ENST00000434679.6:c.*580T= (AVPR2)	ENSP00000393397.1:n.*580T=
ENST00000642393.1:c.97+2244A=
ENST00000646191.1:c.97+2244A=
ENST00000646375.1:c.*98T= (AVPR2)	ENSP00000496396.1:n.*98T=
ENST00000337474.5:c.*98T= (AVPR2)	ENSP00000338072.5:n.*98T=
ENST00000358927.6:c.*98T= (AVPR2)	ENSP00000351805.2:n.*98T=
ENST00000434679.5:c.*580T= (AVPR2)	ENSP00000393397.1:n.*580T=
ENST00000464967.5:n.154+2244A= (L1CAM)
NM_000054.4:c.*98T= (AVPR2)	NP_000045.1:n.*98T=
NM_001146151.1:c.*390T= (AVPR2)	NP_001139623.1:n.*390T=
NR_027419.1:n.1261T= (AVPR2)
XM_006724828.2:c.*98T= (AVPR2)	XP_006724891.1:n.*98T=
NM_000054.5:c.*98T= (AVPR2)	NP_000045.1:n.*98T=
NM_001146151.2:c.*390T= (AVPR2)	NP_001139623.1:n.*390T=
XM_006724828.3:c.*98T= (AVPR2)	XP_006724891.1:n.*98T=
NM_000054.6:c.*98T= (AVPR2)	NP_000045.1:n.*98T=
NM_001146151.3:c.*390T= (AVPR2)	NP_001139623.1:n.*390T=
NR_027419.2:n.1167T= (AVPR2)
NM_000054.7:c.*98T= (AVPR2) MANE Select	NP_000045.1:n.*98T=