Canonical Allele Identifier: CA1594183073
Gene: NIPAL4 HGNC NCBI
ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157463304G= , CM000667.2:g.157463304G= GRCh38
NC_000005.9:g.156890312G= , CM000667.1:g.156890312G= GRCh37
NC_000005.8:g.156822890G= NCBI36
NG_016626.1:g.8286G=

Transcript Alleles

HGVS Amino-acid change
ENST00000311946.8:c.248G= (NIPAL4) MANE Select ENSP00000311687.8:p.Arg83=
ENST00000435489.7:c.248G= (NIPAL4) ENSP00000406456.3:p.Arg83=
ENST00000311946.7:c.434G= (NIPAL4) ENSP00000311687.7:p.Arg145=
ENST00000435489.6:c.434G= (NIPAL4) ENSP00000406456.2:p.Arg145=
ENST00000517951.5:c.*1741+24961C= (ADAM19) ENSP00000428376.1:n.*1741+24961C=
ENST00000519150.1:c.346G= (NIPAL4) ENSP00000430810.1:p.Asp116=
ENST00000519946.1:n.462G= (NIPAL4)
ENST00000521390.5:n.353G= (NIPAL4)
NM_001099287.1:c.434G= (NIPAL4) NP_001092757.1:p.Arg145=
NM_001172292.1:c.434G= (NIPAL4) NP_001165763.1:p.Arg145=
XM_011534552.1:c.-62G= (NIPAL4) XP_011532854.1:n.-62G=
XM_024446043.1:c.-209G= (NIPAL4) XP_024301811.1:n.-209G=
NM_001099287.2:c.248G= (NIPAL4) MANE Select NP_001092757.2:p.Arg83=