Canonical Allele Identifier: CA1594187632

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471785T= , CM000667.2:g.157471785T=	GRCh38
NC_000005.9:g.156898793T= , CM000667.1:g.156898793T=	GRCh37
NC_000005.8:g.156831371T=	NCBI36
NG_016626.1:g.16767T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.554T= (NIPAL4) MANE Select	ENSP00000311687.8:p.Ile185=
ENST00000435489.7:c.497T= (NIPAL4)	ENSP00000406456.3:p.Ile166=
ENST00000311946.7:c.740T= (NIPAL4)	ENSP00000311687.7:p.Ile247=
ENST00000435489.6:c.683T= (NIPAL4)	ENSP00000406456.2:p.Ile228=
ENST00000517951.5:c.*1741+16480A= (ADAM19)	ENSP00000428376.1:n.*1741+16480A=
ENST00000519150.1:c.652T= (NIPAL4)	ENSP00000430810.1:n.652T=
NM_001099287.1:c.740T= (NIPAL4)	NP_001092757.1:p.Ile247=
NM_001172292.1:c.683T= (NIPAL4)	NP_001165763.1:p.Ile228=
XM_011534552.1:c.245T= (NIPAL4)	XP_011532854.1:p.Ile82=
XM_024446043.1:c.41T= (NIPAL4)	XP_024301811.1:p.Ile14=
NM_001099287.2:c.554T= (NIPAL4) MANE Select	NP_001092757.2:p.Ile185=