Canonical Allele Identifier: CA1594187393

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471697C= , CM000667.2:g.157471697C=	GRCh38
NC_000005.9:g.156898705C= , CM000667.1:g.156898705C=	GRCh37
NC_000005.8:g.156831283C=	NCBI36
NG_016626.1:g.16679C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.466C= (NIPAL4) MANE Select	ENSP00000311687.8:p.Leu156=
ENST00000435489.7:c.409C= (NIPAL4)	ENSP00000406456.3:p.Leu137=
ENST00000311946.7:c.652C= (NIPAL4)	ENSP00000311687.7:p.Leu218=
ENST00000435489.6:c.595C= (NIPAL4)	ENSP00000406456.2:p.Leu199=
ENST00000517951.5:c.*1741+16568G= (ADAM19)	ENSP00000428376.1:n.*1741+16568G=
ENST00000519150.1:c.564C= (NIPAL4)	ENSP00000430810.1:n.564C=
NM_001099287.1:c.652C= (NIPAL4)	NP_001092757.1:p.Leu218=
NM_001172292.1:c.595C= (NIPAL4)	NP_001165763.1:p.Leu199=
XM_011534552.1:c.157C= (NIPAL4)	XP_011532854.1:p.Leu53=
XM_024446043.1:c.-48C= (NIPAL4)	XP_024301811.1:n.-48C=
NM_001099287.2:c.466C= (NIPAL4) MANE Select	NP_001092757.2:p.Leu156=