Canonical Allele Identifier: CA2163930226

Gene: NIPA1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.22825318C= , CM000677.2:g.22825318C=	GRCh38
NC_000015.9:g.23047750G= , CM000677.1:g.23047750G=	GRCh37
NC_000015.8:g.20599191G=	NCBI36
NG_009056.1:g.44094C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337435.9:c.*1079C= MANE Select	ENSP00000337452.4:n.*1079C=
ENST00000337435.8:c.*1079C=	ENSP00000337452.4:n.*1079C=
ENST00000437912.6:c.*1079C=	ENSP00000393962.2:n.*1079C=
ENST00000559448.5:c.2041C=
NM_001142275.1:c.*1079C=	NP_001135747.1:n.*1079C=
NM_144599.4:c.*1079C=	NP_653200.2:n.*1079C=
NM_144599.5:c.*1079C= MANE Select	NP_653200.2:n.*1079C=