Canonical Allele Identifier: CA447678231

Gene: NIPAL4 ADAM19

Linked Data

• MyVariant Identifiers: chr5:g.156890328A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463320A>T , CM000667.2:g.157463320A>T	GRCh38
NC_000005.9:g.156890328A>T , CM000667.1:g.156890328A>T	GRCh37
NC_000005.8:g.156822906A>T	NCBI36
NG_016626.1:g.8302A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.264A>T (NIPAL4) MANE Select	ENSP00000311687.8:p.Gly88=
ENST00000435489.7:c.264A>T (NIPAL4)	ENSP00000406456.3:p.Gly88=
ENST00000311946.7:c.450A>T (NIPAL4)	ENSP00000311687.7:p.Gly150=
ENST00000435489.6:c.450A>T (NIPAL4)	ENSP00000406456.2:p.Gly150=
ENST00000517951.5:c.*1741+24945T>A (ADAM19)	ENSP00000428376.1:n.*1741+24945T>A
ENST00000519150.1:c.362A>T (NIPAL4)	ENSP00000430810.1:p.Glu121Val
ENST00000519946.1:n.478A>T (NIPAL4)
ENST00000521390.5:n.369A>T (NIPAL4)
NM_001099287.1:c.450A>T (NIPAL4)	NP_001092757.1:p.Gly150=
NM_001172292.1:c.450A>T (NIPAL4)	NP_001165763.1:p.Gly150=
XM_011534552.1:c.-46A>T (NIPAL4)	XP_011532854.1:n.-46A>T
XM_024446043.1:c.-193A>T (NIPAL4)	XP_024301811.1:n.-193A>T
NM_001099287.2:c.264A>T (NIPAL4) MANE Select	NP_001092757.2:p.Gly88=