Canonical Allele Identifier: CA2960294302
Gene: NIPAL4 HGNC NCBI
ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157471689dup , CM000667.2:g.157471689dup GRCh38
NC_000005.9:g.156898697dup , CM000667.1:g.156898697dup GRCh37
NC_000005.8:g.156831275dup NCBI36
NG_016626.1:g.16671dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000311946.8:c.458dup (NIPAL4) MANE Select ENSP00000311687.8:p.Ser153ArgfsTer26
ENST00000435489.7:c.401dup (NIPAL4) ENSP00000406456.3:p.Ser134ArgfsTer26
ENST00000311946.7:c.644dup (NIPAL4) ENSP00000311687.7:p.Ser215ArgfsTer26
ENST00000435489.6:c.587dup (NIPAL4) ENSP00000406456.2:p.Ser196ArgfsTer26
ENST00000517951.5:c.*1741+16576dup (ADAM19) ENSP00000428376.1:n.*1741+16576dup
ENST00000519150.1:c.556dup (NIPAL4) ENSP00000430810.1:n.556dup
NM_001099287.1:c.644dup (NIPAL4) NP_001092757.1:p.Ser215ArgfsTer26
NM_001172292.1:c.587dup (NIPAL4) NP_001165763.1:p.Ser196ArgfsTer26
XM_011534552.1:c.149dup (NIPAL4) XP_011532854.1:p.Ser50ArgfsTer26
XM_024446043.1:c.-56dup (NIPAL4) XP_024301811.1:n.-56dup
NM_001099287.2:c.458dup (NIPAL4) MANE Select NP_001092757.2:p.Ser153ArgfsTer26