Canonical Allele Identifier: CA1594183007

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463134G= , CM000667.2:g.157463134G=	GRCh38
NC_000005.9:g.156890142G= , CM000667.1:g.156890142G=	GRCh37
NC_000005.8:g.156822720G=	NCBI36
NG_016626.1:g.8116G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.78G= (NIPAL4) MANE Select	ENSP00000311687.8:p.Leu26=
ENST00000435489.7:c.78G= (NIPAL4)	ENSP00000406456.3:p.Leu26=
ENST00000311946.7:c.264G= (NIPAL4)	ENSP00000311687.7:p.Leu88=
ENST00000435489.6:c.264G= (NIPAL4)	ENSP00000406456.2:p.Leu88=
ENST00000517951.5:c.*1741+25131C= (ADAM19)	ENSP00000428376.1:n.*1741+25131C=
ENST00000519150.1:c.176G= (NIPAL4)	ENSP00000430810.1:p.Cys59=
ENST00000519946.1:n.292G= (NIPAL4)
ENST00000521390.5:n.183G= (NIPAL4)
NM_001099287.1:c.264G= (NIPAL4)	NP_001092757.1:p.Leu88=
NM_001172292.1:c.264G= (NIPAL4)	NP_001165763.1:p.Leu88=
XM_011534552.1:c.-232G= (NIPAL4)	XP_011532854.1:n.-232G=
XM_024446043.1:c.-379G= (NIPAL4)	XP_024301811.1:n.-379G=
NM_001099287.2:c.78G= (NIPAL4) MANE Select	NP_001092757.2:p.Leu26=