Canonical Allele Identifier: CA1594187373

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471686A= , CM000667.2:g.157471686A=	GRCh38
NC_000005.9:g.156898694A= , CM000667.1:g.156898694A=	GRCh37
NC_000005.8:g.156831272A=	NCBI36
NG_016626.1:g.16668A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.455A= (NIPAL4) MANE Select	ENSP00000311687.8:p.Glu152=
ENST00000435489.7:c.398A= (NIPAL4)	ENSP00000406456.3:p.Glu133=
ENST00000311946.7:c.641A= (NIPAL4)	ENSP00000311687.7:p.Glu214=
ENST00000435489.6:c.584A= (NIPAL4)	ENSP00000406456.2:p.Glu195=
ENST00000517951.5:c.*1741+16579T= (ADAM19)	ENSP00000428376.1:n.*1741+16579T=
ENST00000519150.1:c.553A= (NIPAL4)	ENSP00000430810.1:n.553A=
NM_001099287.1:c.641A= (NIPAL4)	NP_001092757.1:p.Glu214=
NM_001172292.1:c.584A= (NIPAL4)	NP_001165763.1:p.Glu195=
XM_011534552.1:c.146A= (NIPAL4)	XP_011532854.1:p.Glu49=
XM_024446043.1:c.-59A= (NIPAL4)	XP_024301811.1:n.-59A=
NM_001099287.2:c.455A= (NIPAL4) MANE Select	NP_001092757.2:p.Glu152=