Canonical Allele Identifier: CA2155664378

Gene: PRIMA1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93738999G= , CM000676.2:g.93738999G=	GRCh38
NC_000014.8:g.94205345G= , CM000676.1:g.94205345G=	GRCh37
NC_000014.7:g.93275098G=	NCBI36
NG_009069.1:g.54422C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393140.6:c.230-1629C= MANE Select	ENSP00000376848.1:n.230-1629C=
ENST00000316227.3:c.230-1629C=	ENSP00000320948.3:n.230-1629C=
ENST00000393140.5:c.230-1629C=	ENSP00000376848.1:n.230-1629C=
ENST00000393143.5:c.230-1629C=	ENSP00000376851.1:n.230-1629C=
ENST00000477603.5:c.230-1629C=	ENSP00000434370.1:n.230-1629C=
NM_178013.3:c.230-1629C=	NP_821092.1:n.230-1629C=
XM_011536456.1:c.230-1629C=	XP_011534758.1:n.230-1629C=
XM_011536456.2:c.230-1629C=	XP_011534758.1:n.230-1629C=
XM_024449482.1:c.230-1629C=	XP_024305250.1:n.230-1629C=
XR_002957532.1:n.338-1629C=
XR_002957533.1:n.338-1629C=
NM_178013.4:c.230-1629C= MANE Select	NP_821092.1:n.230-1629C=