Canonical Allele Identifier: CA1594187386

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471689G= , CM000667.2:g.157471689G=	GRCh38
NC_000005.9:g.156898697G= , CM000667.1:g.156898697G=	GRCh37
NC_000005.8:g.156831275G=	NCBI36
NG_016626.1:g.16671G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.458G= (NIPAL4) MANE Select	ENSP00000311687.8:p.Ser153=
ENST00000435489.7:c.401G= (NIPAL4)	ENSP00000406456.3:p.Ser134=
ENST00000311946.7:c.644G= (NIPAL4)	ENSP00000311687.7:p.Ser215=
ENST00000435489.6:c.587G= (NIPAL4)	ENSP00000406456.2:p.Ser196=
ENST00000517951.5:c.*1741+16576C= (ADAM19)	ENSP00000428376.1:n.*1741+16576C=
ENST00000519150.1:c.556G= (NIPAL4)	ENSP00000430810.1:n.556G=
NM_001099287.1:c.644G= (NIPAL4)	NP_001092757.1:p.Ser215=
NM_001172292.1:c.587G= (NIPAL4)	NP_001165763.1:p.Ser196=
XM_011534552.1:c.149G= (NIPAL4)	XP_011532854.1:p.Ser50=
XM_024446043.1:c.-56G= (NIPAL4)	XP_024301811.1:n.-56G=
NM_001099287.2:c.458G= (NIPAL4) MANE Select	NP_001092757.2:p.Ser153=