Canonical Allele Identifier: CA361980382

Gene: NIPAL4 ADAM19

Linked Data

• MyVariant Identifiers: chr5:g.156890341G>A (hg19) ; chr5:g.157463333G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463333G>A , CM000667.2:g.157463333G>A	GRCh38
NC_000005.9:g.156890341G>A , CM000667.1:g.156890341G>A	GRCh37
NC_000005.8:g.156822919G>A	NCBI36
NG_016626.1:g.8315G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.277G>A (NIPAL4) MANE Select	ENSP00000311687.8:p.Val93Met
ENST00000435489.7:c.277G>A (NIPAL4)	ENSP00000406456.3:p.Val93Met
ENST00000311946.7:c.463G>A (NIPAL4)	ENSP00000311687.7:p.Val155Met
ENST00000435489.6:c.463G>A (NIPAL4)	ENSP00000406456.2:p.Val155Met
ENST00000517951.5:c.*1741+24932C>T (ADAM19)	ENSP00000428376.1:n.*1741+24932C>T
ENST00000519150.1:c.375G>A (NIPAL4)	ENSP00000430810.1:p.Leu125=
ENST00000519946.1:n.491G>A (NIPAL4)
ENST00000521390.5:n.382G>A (NIPAL4)
NM_001099287.1:c.463G>A (NIPAL4)	NP_001092757.1:p.Val155Met
NM_001172292.1:c.463G>A (NIPAL4)	NP_001165763.1:p.Val155Met
XM_011534552.1:c.-33G>A (NIPAL4)	XP_011532854.1:n.-33G>A
XM_024446043.1:c.-180G>A (NIPAL4)	XP_024301811.1:n.-180G>A
NM_001099287.2:c.277G>A (NIPAL4) MANE Select	NP_001092757.2:p.Val93Met