Canonical Allele Identifier: CA2346405614

Gene: AVP

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.3083172G= , CM000682.2:g.3083172G=	GRCh38
NC_000020.10:g.3063818G= , CM000682.1:g.3063818G=	GRCh37
NC_000020.9:g.3011818G=	NCBI36
NG_008663.1:g.6553C= , LRG_715:g.6553C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380293.3:c.127C= MANE Select	ENSP00000369647.3:p.Pro43=
NM_000490.4:c.127C= , LRG_715t1:c.127C=	NP_000481.2:p.Pro43=
XM_011529267.1:c.127C=	XP_011527569.1:p.Pro43=
XM_011529267.2:c.127C=	XP_011527569.1:p.Pro43=
NM_000490.5:c.127C= MANE Select	NP_000481.2:p.Pro43=