Canonical Allele Identifier: CA2466520876

Gene: AVPR2 L1CAM

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153906688C= , CM000685.2:g.153906688C=	GRCh38
NC_000023.10:g.153172142C= , CM000685.1:g.153172142C=	GRCh37
NC_000023.9:g.152825336C=	NCBI36
NG_008687.1:g.6715C=
NG_009645.3:g.7536G=
NG_013220.1:g.24573G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646375.2:c.1076C= (AVPR2) MANE Select	ENSP00000496396.1:p.Thr359=
ENST00000434679.6:c.*442C= (AVPR2)	ENSP00000393397.1:n.*442C=
ENST00000642393.1:c.97+2382G=
ENST00000646191.1:c.97+2382G=
ENST00000646375.1:c.1076C= (AVPR2)	ENSP00000496396.1:p.Thr359=
ENST00000337474.5:c.1076C= (AVPR2)	ENSP00000338072.5:p.Thr359=
ENST00000358927.6:c.1076C= (AVPR2)	ENSP00000351805.2:p.Thr359=
ENST00000370049.1:c.*252C= (AVPR2)	ENSP00000359066.1:n.*252C=
ENST00000430697.1:c.988C= (AVPR2)	ENSP00000393513.1:p.Pro330=
ENST00000434679.5:c.*442C= (AVPR2)	ENSP00000393397.1:n.*442C=
ENST00000464967.5:n.154+2382G= (L1CAM)
NM_000054.4:c.1076C= (AVPR2)	NP_000045.1:p.Thr359=
NM_001146151.1:c.*252C= (AVPR2)	NP_001139623.1:n.*252C=
NR_027419.1:n.1123C= (AVPR2)
XM_006724828.2:c.1076C= (AVPR2)	XP_006724891.1:p.Thr359=
NM_000054.5:c.1076C= (AVPR2)	NP_000045.1:p.Thr359=
NM_001146151.2:c.*252C= (AVPR2)	NP_001139623.1:n.*252C=
XM_006724828.3:c.1076C= (AVPR2)	XP_006724891.1:p.Thr359=
NM_000054.6:c.1076C= (AVPR2)	NP_000045.1:p.Thr359=
NM_001146151.3:c.*252C= (AVPR2)	NP_001139623.1:n.*252C=
NR_027419.2:n.1029C= (AVPR2)
NM_000054.7:c.1076C= (AVPR2) MANE Select	NP_000045.1:p.Thr359=