Canonical Allele Identifier: CA447678235

Gene: NIPAL4 ADAM19

Linked Data

• MyVariant Identifiers: chr5:g.156890331C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.157463323C>T , CM000667.2:g.157463323C>T	GRCh38
NC_000005.9:g.156890331C>T , CM000667.1:g.156890331C>T	GRCh37
NC_000005.8:g.156822909C>T	NCBI36
NG_016626.1:g.8305C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000311946.8:c.267C>T (NIPAL4) MANE Select	ENSP00000311687.8:p.Ala89=
ENST00000435489.7:c.267C>T (NIPAL4)	ENSP00000406456.3:p.Ala89=
ENST00000311946.7:c.453C>T (NIPAL4)	ENSP00000311687.7:p.Ala151=
ENST00000435489.6:c.453C>T (NIPAL4)	ENSP00000406456.2:p.Ala151=
ENST00000517951.5:c.*1741+24942G>A (ADAM19)	ENSP00000428376.1:n.*1741+24942G>A
ENST00000519150.1:c.365C>T (NIPAL4)	ENSP00000430810.1:p.Pro122Leu
ENST00000519946.1:n.481C>T (NIPAL4)
ENST00000521390.5:n.372C>T (NIPAL4)
NM_001099287.1:c.453C>T (NIPAL4)	NP_001092757.1:p.Ala151=
NM_001172292.1:c.453C>T (NIPAL4)	NP_001165763.1:p.Ala151=
XM_011534552.1:c.-43C>T (NIPAL4)	XP_011532854.1:n.-43C>T
XM_024446043.1:c.-190C>T (NIPAL4)	XP_024301811.1:n.-190C>T
NM_001099287.2:c.267C>T (NIPAL4) MANE Select	NP_001092757.2:p.Ala89=