Canonical Allele Identifier: CA1594187643

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471788T= , CM000667.2:g.157471788T=	GRCh38
NC_000005.9:g.156898796T= , CM000667.1:g.156898796T=	GRCh37
NC_000005.8:g.156831374T=	NCBI36
NG_016626.1:g.16770T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.557T= (NIPAL4) MANE Select	ENSP00000311687.8:p.Met186=
ENST00000435489.7:c.500T= (NIPAL4)	ENSP00000406456.3:p.Met167=
ENST00000311946.7:c.743T= (NIPAL4)	ENSP00000311687.7:p.Met248=
ENST00000435489.6:c.686T= (NIPAL4)	ENSP00000406456.2:p.Met229=
ENST00000517951.5:c.*1741+16477A= (ADAM19)	ENSP00000428376.1:n.*1741+16477A=
ENST00000519150.1:c.655T= (NIPAL4)	ENSP00000430810.1:n.655T=
NM_001099287.1:c.743T= (NIPAL4)	NP_001092757.1:p.Met248=
NM_001172292.1:c.686T= (NIPAL4)	NP_001165763.1:p.Met229=
XM_011534552.1:c.248T= (NIPAL4)	XP_011532854.1:p.Met83=
XM_024446043.1:c.44T= (NIPAL4)	XP_024301811.1:p.Met15=
NM_001099287.2:c.557T= (NIPAL4) MANE Select	NP_001092757.2:p.Met186=