Canonical Allele Identifier: CA1594182968

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463052T= , CM000667.2:g.157463052T=	GRCh38
NC_000005.9:g.156890060T= , CM000667.1:g.156890060T=	GRCh37
NC_000005.8:g.156822638T=	NCBI36
NG_016626.1:g.8034T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.38-42T= (NIPAL4) MANE Select	ENSP00000311687.8:n.38-42T=
ENST00000435489.7:c.38-42T= (NIPAL4)	ENSP00000406456.3:n.38-42T=
ENST00000311946.7:c.224-42T= (NIPAL4)	ENSP00000311687.7:n.224-42T=
ENST00000435489.6:c.224-42T= (NIPAL4)	ENSP00000406456.2:n.224-42T=
ENST00000517951.5:c.*1741+25213A= (ADAM19)	ENSP00000428376.1:n.*1741+25213A=
ENST00000519150.1:c.136-42T= (NIPAL4)	ENSP00000430810.1:n.136-42T=
ENST00000519946.1:n.252-42T= (NIPAL4)
ENST00000521390.5:n.143-42T= (NIPAL4)
NM_001099287.1:c.224-42T= (NIPAL4)	NP_001092757.1:n.224-42T=
NM_001172292.1:c.224-42T= (NIPAL4)	NP_001165763.1:n.224-42T=
XM_011534552.1:c.-272-42T= (NIPAL4)	XP_011532854.1:n.-272-42T=
XM_024446043.1:c.-419-42T= (NIPAL4)	XP_024301811.1:n.-419-42T=
NM_001099287.2:c.38-42T= (NIPAL4) MANE Select	NP_001092757.2:n.38-42T=