Canonical Allele Identifier: CA1594183033
Gene: NIPAL4 HGNC NCBI
ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157463206C= , CM000667.2:g.157463206C= GRCh38
NC_000005.9:g.156890214C= , CM000667.1:g.156890214C= GRCh37
NC_000005.8:g.156822792C= NCBI36
NG_016626.1:g.8188C=

Transcript Alleles

HGVS Amino-acid change
ENST00000311946.8:c.150C= (NIPAL4) MANE Select ENSP00000311687.8:p.Ile50=
ENST00000435489.7:c.150C= (NIPAL4) ENSP00000406456.3:p.Ile50=
ENST00000311946.7:c.336C= (NIPAL4) ENSP00000311687.7:p.Ile112=
ENST00000435489.6:c.336C= (NIPAL4) ENSP00000406456.2:p.Ile112=
ENST00000517951.5:c.*1741+25059G= (ADAM19) ENSP00000428376.1:n.*1741+25059G=
ENST00000519150.1:c.248C= (NIPAL4) ENSP00000430810.1:p.Ser83=
ENST00000519946.1:n.364C= (NIPAL4)
ENST00000521390.5:n.255C= (NIPAL4)
NM_001099287.1:c.336C= (NIPAL4) NP_001092757.1:p.Ile112=
NM_001172292.1:c.336C= (NIPAL4) NP_001165763.1:p.Ile112=
XM_011534552.1:c.-160C= (NIPAL4) XP_011532854.1:n.-160C=
XM_024446043.1:c.-307C= (NIPAL4) XP_024301811.1:n.-307C=
NM_001099287.2:c.150C= (NIPAL4) MANE Select NP_001092757.2:p.Ile50=