Canonical Allele Identifier: CA361980341

Gene: NIPAL4 ADAM19

Linked Data

• MyVariant Identifiers: chr5:g.156890317G>C (hg19) ; chr5:g.157463309G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463309G>C , CM000667.2:g.157463309G>C	GRCh38
NC_000005.9:g.156890317G>C , CM000667.1:g.156890317G>C	GRCh37
NC_000005.8:g.156822895G>C	NCBI36
NG_016626.1:g.8291G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000311946.8:c.253G>C (NIPAL4) MANE Select	ENSP00000311687.8:p.Val85Leu
ENST00000435489.7:c.253G>C (NIPAL4)	ENSP00000406456.3:p.Val85Leu
ENST00000311946.7:c.439G>C (NIPAL4)	ENSP00000311687.7:p.Val147Leu
ENST00000435489.6:c.439G>C (NIPAL4)	ENSP00000406456.2:p.Val147Leu
ENST00000517951.5:c.*1741+24956C>G (ADAM19)	ENSP00000428376.1:n.*1741+24956C>G
ENST00000519150.1:c.351G>C (NIPAL4)	ENSP00000430810.1:p.Ser117=
ENST00000519946.1:n.467G>C (NIPAL4)
ENST00000521390.5:n.358G>C (NIPAL4)
NM_001099287.1:c.439G>C (NIPAL4)	NP_001092757.1:p.Val147Leu
NM_001172292.1:c.439G>C (NIPAL4)	NP_001165763.1:p.Val147Leu
XM_011534552.1:c.-57G>C (NIPAL4)	XP_011532854.1:n.-57G>C
XM_024446043.1:c.-204G>C (NIPAL4)	XP_024301811.1:n.-204G>C
NM_001099287.2:c.253G>C (NIPAL4) MANE Select	NP_001092757.2:p.Val85Leu