Canonical Allele Identifier: CA361979989

Gene: NIPAL4 ADAM19

Linked Data

• MyVariant Identifiers: chr5:g.156890176C>A (hg19) ; chr5:g.157463168C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463168C>A , CM000667.2:g.157463168C>A	GRCh38
NC_000005.9:g.156890176C>A , CM000667.1:g.156890176C>A	GRCh37
NC_000005.8:g.156822754C>A	NCBI36
NG_016626.1:g.8150C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.112C>A (NIPAL4) MANE Select	ENSP00000311687.8:p.Pro38Thr
ENST00000435489.7:c.112C>A (NIPAL4)	ENSP00000406456.3:p.Pro38Thr
ENST00000311946.7:c.298C>A (NIPAL4)	ENSP00000311687.7:p.Pro100Thr
ENST00000435489.6:c.298C>A (NIPAL4)	ENSP00000406456.2:p.Pro100Thr
ENST00000517951.5:c.*1741+25097G>T (ADAM19)	ENSP00000428376.1:n.*1741+25097G>T
ENST00000519150.1:c.210C>A (NIPAL4)	ENSP00000430810.1:p.Cys70Ter
ENST00000519946.1:n.326C>A (NIPAL4)
ENST00000521390.5:n.217C>A (NIPAL4)
NM_001099287.1:c.298C>A (NIPAL4)	NP_001092757.1:p.Pro100Thr
NM_001172292.1:c.298C>A (NIPAL4)	NP_001165763.1:p.Pro100Thr
XM_011534552.1:c.-198C>A (NIPAL4)	XP_011532854.1:n.-198C>A
XM_024446043.1:c.-345C>A (NIPAL4)	XP_024301811.1:n.-345C>A
NM_001099287.2:c.112C>A (NIPAL4) MANE Select	NP_001092757.2:p.Pro38Thr