Canonical Allele Identifier: CA2840809989

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463033dup , CM000667.2:g.157463033dup	GRCh38
NC_000005.9:g.156890041dup , CM000667.1:g.156890041dup	GRCh37
NC_000005.8:g.156822619dup	NCBI36
NG_016626.1:g.8015dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.38-61dup (NIPAL4) MANE Select	ENSP00000311687.8:n.38-61dup
ENST00000435489.7:c.38-61dup (NIPAL4)	ENSP00000406456.3:n.38-61dup
ENST00000311946.7:c.224-61dup (NIPAL4)	ENSP00000311687.7:n.224-61dup
ENST00000435489.6:c.224-61dup (NIPAL4)	ENSP00000406456.2:n.224-61dup
ENST00000517951.5:c.*1741+25233dup (ADAM19)	ENSP00000428376.1:n.*1741+25233dup
ENST00000519150.1:c.136-61dup (NIPAL4)	ENSP00000430810.1:n.136-61dup
ENST00000519946.1:n.252-61dup (NIPAL4)
ENST00000521390.5:n.143-61dup (NIPAL4)
NM_001099287.1:c.224-61dup (NIPAL4)	NP_001092757.1:n.224-61dup
NM_001172292.1:c.224-61dup (NIPAL4)	NP_001165763.1:n.224-61dup
XM_011534552.1:c.-272-61dup (NIPAL4)	XP_011532854.1:n.-272-61dup
XM_024446043.1:c.-419-61dup (NIPAL4)	XP_024301811.1:n.-419-61dup
NM_001099287.2:c.38-61dup (NIPAL4) MANE Select	NP_001092757.2:n.38-61dup