Canonical Allele Identifier: CA3133954010
Community Standard Title: NM_001099287.2(NIPAL4):c.426-58T=
Gene: NIPAL4 HGNC NCBI
ADAM19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157471599T= , CM000667.2:g.157471599T= GRCh38
NC_000005.9:g.156898607T= , CM000667.1:g.156898607T= GRCh37
NC_000005.8:g.156831185T= NCBI36
NG_016626.1:g.16581T=

Transcript Alleles

HGVS Amino-acid Change
NM_001099287.2:c.426-58T= (NIPAL4) MANE Select NP_001092757.2:n.426-58T=
ENST00000311946.8:c.426-58T= (NIPAL4) MANE Select ENSP00000311687.8:n.426-58T=
NM_001099287.1:c.612-58T= (NIPAL4) NP_001092757.1:n.612-58T=
NM_001172292.1:c.555-58T= (NIPAL4) NP_001165763.1:n.555-58T=
ENST00000311946.7:c.612-58T= (NIPAL4) ENSP00000311687.7:n.612-58T=
ENST00000435489.6:c.555-58T= (NIPAL4) ENSP00000406456.2:n.555-58T=
ENST00000435489.7:c.369-58T= (NIPAL4) ENSP00000406456.3:n.369-58T=
ENST00000517951.5:c.*1741+16666A= (ADAM19) ENSP00000428376.1:n.*1741+16666A=
ENST00000519150.1:c.524-58T= (NIPAL4) ENSP00000430810.1:n.524-58T=
XM_011534552.1:c.117-58T= (NIPAL4) XP_011532854.1:n.117-58T=
XM_024446043.1:c.-88-58T= (NIPAL4) XP_024301811.1:n.-88-58T=