Canonical Allele Identifier: CA361972766
Gene: NIPAL4 HGNC NCBI
ADAM19 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000311946.8:c.550A>T (NIPAL4) MANE Select ENSP00000311687.8:p.Thr184Ser
ENST00000435489.7:c.493A>T (NIPAL4) ENSP00000406456.3:p.Thr165Ser
ENST00000311946.7:c.736A>T (NIPAL4) ENSP00000311687.7:p.Thr246Ser
ENST00000435489.6:c.679A>T (NIPAL4) ENSP00000406456.2:p.Thr227Ser
ENST00000517951.5:c.*1741+16484T>A (ADAM19) ENSP00000428376.1:n.*1741+16484T>A
ENST00000519150.1:c.648A>T (NIPAL4) ENSP00000430810.1:n.648A>T
NM_001099287.1:c.736A>T (NIPAL4) NP_001092757.1:p.Thr246Ser
NM_001172292.1:c.679A>T (NIPAL4) NP_001165763.1:p.Thr227Ser
XM_011534552.1:c.241A>T (NIPAL4) XP_011532854.1:p.Thr81Ser
XM_024446043.1:c.37A>T (NIPAL4) XP_024301811.1:p.Thr13Ser
NM_001099287.2:c.550A>T (NIPAL4) MANE Select NP_001092757.2:p.Thr184Ser