Canonical Allele Identifier: CA447676998

Gene: NIPAL4 ADAM19

Linked Data

• MyVariant Identifiers: chr5:g.156890190C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463182C>G , CM000667.2:g.157463182C>G	GRCh38
NC_000005.9:g.156890190C>G , CM000667.1:g.156890190C>G	GRCh37
NC_000005.8:g.156822768C>G	NCBI36
NG_016626.1:g.8164C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.126C>G (NIPAL4) MANE Select	ENSP00000311687.8:p.Thr42=
ENST00000435489.7:c.126C>G (NIPAL4)	ENSP00000406456.3:p.Thr42=
ENST00000311946.7:c.312C>G (NIPAL4)	ENSP00000311687.7:p.Thr104=
ENST00000435489.6:c.312C>G (NIPAL4)	ENSP00000406456.2:p.Thr104=
ENST00000517951.5:c.*1741+25083G>C (ADAM19)	ENSP00000428376.1:n.*1741+25083G>C
ENST00000519150.1:c.224C>G (NIPAL4)	ENSP00000430810.1:p.Pro75Arg
ENST00000519946.1:n.340C>G (NIPAL4)
ENST00000521390.5:n.231C>G (NIPAL4)
NM_001099287.1:c.312C>G (NIPAL4)	NP_001092757.1:p.Thr104=
NM_001172292.1:c.312C>G (NIPAL4)	NP_001165763.1:p.Thr104=
XM_011534552.1:c.-184C>G (NIPAL4)	XP_011532854.1:n.-184C>G
XM_024446043.1:c.-331C>G (NIPAL4)	XP_024301811.1:n.-331C>G
NM_001099287.2:c.126C>G (NIPAL4) MANE Select	NP_001092757.2:p.Thr42=