Canonical Allele Identifier: CA447678238

Gene: NIPAL4 ADAM19

Linked Data

• MyVariant Identifiers: chr5:g.156890334T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463326T>G , CM000667.2:g.157463326T>G	GRCh38
NC_000005.9:g.156890334T>G , CM000667.1:g.156890334T>G	GRCh37
NC_000005.8:g.156822912T>G	NCBI36
NG_016626.1:g.8308T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.270T>G (NIPAL4) MANE Select	ENSP00000311687.8:p.Thr90=
ENST00000435489.7:c.270T>G (NIPAL4)	ENSP00000406456.3:p.Thr90=
ENST00000311946.7:c.456T>G (NIPAL4)	ENSP00000311687.7:p.Thr152=
ENST00000435489.6:c.456T>G (NIPAL4)	ENSP00000406456.2:p.Thr152=
ENST00000517951.5:c.*1741+24939A>C (ADAM19)	ENSP00000428376.1:n.*1741+24939A>C
ENST00000519150.1:c.368T>G (NIPAL4)	ENSP00000430810.1:p.Leu123Arg
ENST00000519946.1:n.484T>G (NIPAL4)
ENST00000521390.5:n.375T>G (NIPAL4)
NM_001099287.1:c.456T>G (NIPAL4)	NP_001092757.1:p.Thr152=
NM_001172292.1:c.456T>G (NIPAL4)	NP_001165763.1:p.Thr152=
XM_011534552.1:c.-40T>G (NIPAL4)	XP_011532854.1:n.-40T>G
XM_024446043.1:c.-187T>G (NIPAL4)	XP_024301811.1:n.-187T>G
NM_001099287.2:c.270T>G (NIPAL4) MANE Select	NP_001092757.2:p.Thr90=