Canonical Allele Identifier: CA361980218
Gene: NIPAL4 HGNC NCBI
ADAM19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157463249C>A , CM000667.2:g.157463249C>A GRCh38
NC_000005.9:g.156890257C>A , CM000667.1:g.156890257C>A GRCh37
NC_000005.8:g.156822835C>A NCBI36
NG_016626.1:g.8231C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000311946.8:c.193C>A (NIPAL4) MANE Select ENSP00000311687.8:p.Leu65Met
ENST00000435489.7:c.193C>A (NIPAL4) ENSP00000406456.3:p.Leu65Met
ENST00000311946.7:c.379C>A (NIPAL4) ENSP00000311687.7:p.Leu127Met
ENST00000435489.6:c.379C>A (NIPAL4) ENSP00000406456.2:p.Leu127Met
ENST00000517951.5:c.*1741+25016G>T (ADAM19) ENSP00000428376.1:n.*1741+25016G>T
ENST00000519150.1:c.291C>A (NIPAL4) ENSP00000430810.1:p.Ser97=
ENST00000519946.1:n.407C>A (NIPAL4)
ENST00000521390.5:n.298C>A (NIPAL4)
NM_001099287.1:c.379C>A (NIPAL4) NP_001092757.1:p.Leu127Met
NM_001172292.1:c.379C>A (NIPAL4) NP_001165763.1:p.Leu127Met
XM_011534552.1:c.-117C>A (NIPAL4) XP_011532854.1:n.-117C>A
XM_024446043.1:c.-264C>A (NIPAL4) XP_024301811.1:n.-264C>A
NM_001099287.2:c.193C>A (NIPAL4) MANE Select NP_001092757.2:p.Leu65Met