Canonical Allele Identifier: CA2960294291

Gene: NIPAL4 ADAM19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157471592A>C , CM000667.2:g.157471592A>C	GRCh38
NC_000005.9:g.156898600A>C , CM000667.1:g.156898600A>C	GRCh37
NC_000005.8:g.156831178A>C	NCBI36
NG_016626.1:g.16574A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.426-65A>C (NIPAL4) MANE Select	ENSP00000311687.8:n.426-65A>C
ENST00000435489.7:c.369-65A>C (NIPAL4)	ENSP00000406456.3:n.369-65A>C
ENST00000311946.7:c.612-65A>C (NIPAL4)	ENSP00000311687.7:n.612-65A>C
ENST00000435489.6:c.555-65A>C (NIPAL4)	ENSP00000406456.2:n.555-65A>C
ENST00000517951.5:c.*1741+16673T>G (ADAM19)	ENSP00000428376.1:n.*1741+16673T>G
ENST00000519150.1:c.524-65A>C (NIPAL4)	ENSP00000430810.1:n.524-65A>C
NM_001099287.1:c.612-65A>C (NIPAL4)	NP_001092757.1:n.612-65A>C
NM_001172292.1:c.555-65A>C (NIPAL4)	NP_001165763.1:n.555-65A>C
XM_011534552.1:c.117-65A>C (NIPAL4)	XP_011532854.1:n.117-65A>C
XM_024446043.1:c.-88-65A>C (NIPAL4)	XP_024301811.1:n.-88-65A>C
NM_001099287.2:c.426-65A>C (NIPAL4) MANE Select	NP_001092757.2:n.426-65A>C