Canonical Allele Identifier: CA2466520956

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906879C= , CM000685.2:g.153906879C=	GRCh38
NC_000023.10:g.153172333C= , CM000685.1:g.153172333C=	GRCh37
NC_000023.9:g.152825527C=	NCBI36
NG_008687.1:g.6906C=
NG_009645.3:g.7345G=
NG_013220.1:g.24382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.*151C= (AVPR2) MANE Select	ENSP00000496396.1:n.*151C=
ENST00000434679.6:c.*633C= (AVPR2)	ENSP00000393397.1:n.*633C=
ENST00000642393.1:c.97+2191G=
ENST00000646191.1:c.97+2191G=
ENST00000646375.1:c.*151C= (AVPR2)	ENSP00000496396.1:n.*151C=
ENST00000337474.5:c.*151C= (AVPR2)	ENSP00000338072.5:n.*151C=
ENST00000358927.6:c.*151C= (AVPR2)	ENSP00000351805.2:n.*151C=
ENST00000434679.5:c.*633C= (AVPR2)	ENSP00000393397.1:n.*633C=
ENST00000464967.5:n.154+2191G= (L1CAM)
NM_000054.4:c.*151C= (AVPR2)	NP_000045.1:n.*151C=
NM_001146151.1:c.*443C= (AVPR2)	NP_001139623.1:n.*443C=
NR_027419.1:n.1314C= (AVPR2)
XM_006724828.2:c.*151C= (AVPR2)	XP_006724891.1:n.*151C=
NM_000054.5:c.*151C= (AVPR2)	NP_000045.1:n.*151C=
NM_001146151.2:c.*443C= (AVPR2)	NP_001139623.1:n.*443C=
XM_006724828.3:c.*151C= (AVPR2)	XP_006724891.1:n.*151C=
NM_000054.6:c.*151C= (AVPR2)	NP_000045.1:n.*151C=
NM_001146151.3:c.*443C= (AVPR2)	NP_001139623.1:n.*443C=
NR_027419.2:n.1220C= (AVPR2)
NM_000054.7:c.*151C= (AVPR2) MANE Select	NP_000045.1:n.*151C=