Canonical Allele Identifier: CA1594187654

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471793A= , CM000667.2:g.157471793A=	GRCh38
NC_000005.9:g.156898801A= , CM000667.1:g.156898801A=	GRCh37
NC_000005.8:g.156831379A=	NCBI36
NG_016626.1:g.16775A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.562A= (NIPAL4) MANE Select	ENSP00000311687.8:p.Met188=
ENST00000435489.7:c.505A= (NIPAL4)	ENSP00000406456.3:p.Met169=
ENST00000311946.7:c.748A= (NIPAL4)	ENSP00000311687.7:p.Met250=
ENST00000435489.6:c.691A= (NIPAL4)	ENSP00000406456.2:p.Met231=
ENST00000517951.5:c.*1741+16472T= (ADAM19)	ENSP00000428376.1:n.*1741+16472T=
ENST00000519150.1:c.660A= (NIPAL4)	ENSP00000430810.1:n.660A=
NM_001099287.1:c.748A= (NIPAL4)	NP_001092757.1:p.Met250=
NM_001172292.1:c.691A= (NIPAL4)	NP_001165763.1:p.Met231=
XM_011534552.1:c.253A= (NIPAL4)	XP_011532854.1:p.Met85=
XM_024446043.1:c.49A= (NIPAL4)	XP_024301811.1:p.Met17=
NM_001099287.2:c.562A= (NIPAL4) MANE Select	NP_001092757.2:p.Met188=