Canonical Allele Identifier: CA447676990

Gene: NIPAL4 ADAM19

Linked Data

• MyVariant Identifiers: chr5:g.156890184T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463176T>C , CM000667.2:g.157463176T>C	GRCh38
NC_000005.9:g.156890184T>C , CM000667.1:g.156890184T>C	GRCh37
NC_000005.8:g.156822762T>C	NCBI36
NG_016626.1:g.8158T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.120T>C (NIPAL4) MANE Select	ENSP00000311687.8:p.Asn40=
ENST00000435489.7:c.120T>C (NIPAL4)	ENSP00000406456.3:p.Asn40=
ENST00000311946.7:c.306T>C (NIPAL4)	ENSP00000311687.7:p.Asn102=
ENST00000435489.6:c.306T>C (NIPAL4)	ENSP00000406456.2:p.Asn102=
ENST00000517951.5:c.*1741+25089A>G (ADAM19)	ENSP00000428376.1:n.*1741+25089A>G
ENST00000519150.1:c.218T>C (NIPAL4)	ENSP00000430810.1:p.Met73Thr
ENST00000519946.1:n.334T>C (NIPAL4)
ENST00000521390.5:n.225T>C (NIPAL4)
NM_001099287.1:c.306T>C (NIPAL4)	NP_001092757.1:p.Asn102=
NM_001172292.1:c.306T>C (NIPAL4)	NP_001165763.1:p.Asn102=
XM_011534552.1:c.-190T>C (NIPAL4)	XP_011532854.1:n.-190T>C
XM_024446043.1:c.-337T>C (NIPAL4)	XP_024301811.1:n.-337T>C
NM_001099287.2:c.120T>C (NIPAL4) MANE Select	NP_001092757.2:p.Asn40=