Canonical Allele Identifier: CA1594187655

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471801C= , CM000667.2:g.157471801C=	GRCh38
NC_000005.9:g.156898809C= , CM000667.1:g.156898809C=	GRCh37
NC_000005.8:g.156831387C=	NCBI36
NG_016626.1:g.16783C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.570C= (NIPAL4) MANE Select	ENSP00000311687.8:p.Ser190=
ENST00000435489.7:c.513C= (NIPAL4)	ENSP00000406456.3:p.Ser171=
ENST00000311946.7:c.756C= (NIPAL4)	ENSP00000311687.7:p.Ser252=
ENST00000435489.6:c.699C= (NIPAL4)	ENSP00000406456.2:p.Ser233=
ENST00000517951.5:c.*1741+16464G= (ADAM19)	ENSP00000428376.1:n.*1741+16464G=
ENST00000519150.1:c.668C= (NIPAL4)	ENSP00000430810.1:n.668C=
NM_001099287.1:c.756C= (NIPAL4)	NP_001092757.1:p.Ser252=
NM_001172292.1:c.699C= (NIPAL4)	NP_001165763.1:p.Ser233=
XM_011534552.1:c.261C= (NIPAL4)	XP_011532854.1:p.Ser87=
XM_024446043.1:c.57C= (NIPAL4)	XP_024301811.1:p.Ser19=
NM_001099287.2:c.570C= (NIPAL4) MANE Select	NP_001092757.2:p.Ser190=