Canonical Allele Identifier: CA1594187648

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471790G= , CM000667.2:g.157471790G=	GRCh38
NC_000005.9:g.156898798G= , CM000667.1:g.156898798G=	GRCh37
NC_000005.8:g.156831376G=	NCBI36
NG_016626.1:g.16772G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.559G= (NIPAL4) MANE Select	ENSP00000311687.8:p.Glu187=
ENST00000435489.7:c.502G= (NIPAL4)	ENSP00000406456.3:p.Glu168=
ENST00000311946.7:c.745G= (NIPAL4)	ENSP00000311687.7:p.Glu249=
ENST00000435489.6:c.688G= (NIPAL4)	ENSP00000406456.2:p.Glu230=
ENST00000517951.5:c.*1741+16475C= (ADAM19)	ENSP00000428376.1:n.*1741+16475C=
ENST00000519150.1:c.657G= (NIPAL4)	ENSP00000430810.1:n.657G=
NM_001099287.1:c.745G= (NIPAL4)	NP_001092757.1:p.Glu249=
NM_001172292.1:c.688G= (NIPAL4)	NP_001165763.1:p.Glu230=
XM_011534552.1:c.250G= (NIPAL4)	XP_011532854.1:p.Glu84=
XM_024446043.1:c.46G= (NIPAL4)	XP_024301811.1:p.Glu16=
NM_001099287.2:c.559G= (NIPAL4) MANE Select	NP_001092757.2:p.Glu187=