Canonical Allele Identifier: CA1594183012

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463151_157463152delinsAC , CM000667.2:g.157463151_157463152delinsAC	GRCh38
NC_000005.9:g.156890159_156890160delinsAC , CM000667.1:g.156890159_156890160delinsAC	GRCh37
NC_000005.8:g.156822737_156822738delinsAC	NCBI36
NG_016626.1:g.8133_8134delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.95_96delinsAC (NIPAL4) MANE Select	ENSP00000311687.8:p.Asp32=
ENST00000435489.7:c.95_96delinsAC (NIPAL4)	ENSP00000406456.3:p.Asp32=
ENST00000311946.7:c.281_282delinsAC (NIPAL4)	ENSP00000311687.7:p.Asp94=
ENST00000435489.6:c.281_282delinsAC (NIPAL4)	ENSP00000406456.2:p.Asp94=
ENST00000517951.5:c.*1741+25113_*1741+25114delinsGT (ADAM19)	ENSP00000428376.1:n.*1741+25113_*1741+25114delinsGT
ENST00000519150.1:c.193_194delinsAC (NIPAL4)	ENSP00000430810.1:p.Thr65=
ENST00000519946.1:n.309_310delinsAC (NIPAL4)
ENST00000521390.5:n.200_201delinsAC (NIPAL4)
NM_001099287.1:c.281_282delinsAC (NIPAL4)	NP_001092757.1:p.Asp94=
NM_001172292.1:c.281_282delinsAC (NIPAL4)	NP_001165763.1:p.Asp94=
XM_011534552.1:c.-215_-214delinsAC (NIPAL4)	XP_011532854.1:n.-215_-214delinsAC
XM_024446043.1:c.-362_-361delinsAC (NIPAL4)	XP_024301811.1:n.-362_-361delinsAC
NM_001099287.2:c.95_96delinsAC (NIPAL4) MANE Select	NP_001092757.2:p.Asp32=