Canonical Allele Identifier: CA361972446

Gene: NIPAL4 ADAM19

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471675T>A , CM000667.2:g.157471675T>A	GRCh38
NC_000005.9:g.156898683T>A , CM000667.1:g.156898683T>A	GRCh37
NC_000005.8:g.156831261T>A	NCBI36
NG_016626.1:g.16657T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.444T>A (NIPAL4) MANE Select	ENSP00000311687.8:p.Tyr148Ter
ENST00000435489.7:c.387T>A (NIPAL4)	ENSP00000406456.3:p.Tyr129Ter
ENST00000311946.7:c.630T>A (NIPAL4)	ENSP00000311687.7:p.Tyr210Ter
ENST00000435489.6:c.573T>A (NIPAL4)	ENSP00000406456.2:p.Tyr191Ter
ENST00000517951.5:c.*1741+16590A>T (ADAM19)	ENSP00000428376.1:n.*1741+16590A>T
ENST00000519150.1:c.542T>A (NIPAL4)	ENSP00000430810.1:n.542T>A
NM_001099287.1:c.630T>A (NIPAL4)	NP_001092757.1:p.Tyr210Ter
NM_001172292.1:c.573T>A (NIPAL4)	NP_001165763.1:p.Tyr191Ter
XM_011534552.1:c.135T>A (NIPAL4)	XP_011532854.1:p.Tyr45Ter
XM_024446043.1:c.-70T>A (NIPAL4)	XP_024301811.1:n.-70T>A
NM_001099287.2:c.444T>A (NIPAL4) MANE Select	NP_001092757.2:p.Tyr148Ter