Canonical Allele Identifier: CA1594183013

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463152C= , CM000667.2:g.157463152C=	GRCh38
NC_000005.9:g.156890160C= , CM000667.1:g.156890160C=	GRCh37
NC_000005.8:g.156822738C=	NCBI36
NG_016626.1:g.8134C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.96C= (NIPAL4) MANE Select	ENSP00000311687.8:p.Asp32=
ENST00000435489.7:c.96C= (NIPAL4)	ENSP00000406456.3:p.Asp32=
ENST00000311946.7:c.282C= (NIPAL4)	ENSP00000311687.7:p.Asp94=
ENST00000435489.6:c.282C= (NIPAL4)	ENSP00000406456.2:p.Asp94=
ENST00000517951.5:c.*1741+25113G= (ADAM19)	ENSP00000428376.1:n.*1741+25113G=
ENST00000519150.1:c.194C= (NIPAL4)	ENSP00000430810.1:p.Thr65=
ENST00000519946.1:n.310C= (NIPAL4)
ENST00000521390.5:n.201C= (NIPAL4)
NM_001099287.1:c.282C= (NIPAL4)	NP_001092757.1:p.Asp94=
NM_001172292.1:c.282C= (NIPAL4)	NP_001165763.1:p.Asp94=
XM_011534552.1:c.-214C= (NIPAL4)	XP_011532854.1:n.-214C=
XM_024446043.1:c.-361C= (NIPAL4)	XP_024301811.1:n.-361C=
NM_001099287.2:c.96C= (NIPAL4) MANE Select	NP_001092757.2:p.Asp32=