Canonical Allele Identifier: CA1594187628

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471781A= , CM000667.2:g.157471781A=	GRCh38
NC_000005.9:g.156898789A= , CM000667.1:g.156898789A=	GRCh37
NC_000005.8:g.156831367A=	NCBI36
NG_016626.1:g.16763A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.550A= (NIPAL4) MANE Select	ENSP00000311687.8:p.Thr184=
ENST00000435489.7:c.493A= (NIPAL4)	ENSP00000406456.3:p.Thr165=
ENST00000311946.7:c.736A= (NIPAL4)	ENSP00000311687.7:p.Thr246=
ENST00000435489.6:c.679A= (NIPAL4)	ENSP00000406456.2:p.Thr227=
ENST00000517951.5:c.*1741+16484T= (ADAM19)	ENSP00000428376.1:n.*1741+16484T=
ENST00000519150.1:c.648A= (NIPAL4)	ENSP00000430810.1:n.648A=
NM_001099287.1:c.736A= (NIPAL4)	NP_001092757.1:p.Thr246=
NM_001172292.1:c.679A= (NIPAL4)	NP_001165763.1:p.Thr227=
XM_011534552.1:c.241A= (NIPAL4)	XP_011532854.1:p.Thr81=
XM_024446043.1:c.37A= (NIPAL4)	XP_024301811.1:p.Thr13=
NM_001099287.2:c.550A= (NIPAL4) MANE Select	NP_001092757.2:p.Thr184=