Canonical Allele Identifier: CA16090513

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15167440T>G , CM000664.2:g.15167440T>G	GRCh38
NC_000002.11:g.15307564T>G , CM000664.1:g.15307564T>G	GRCh37
NC_000002.10:g.15225015T>G	NCBI36
NG_032964.1:g.398909A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015909.4:c.6841-117A>C MANE Select	NP_056993.2:n.6841-117A>C
ENST00000281513.10:c.6841-117A>C MANE Select	ENSP00000281513.5:n.6841-117A>C
NM_015909.3:c.6841-117A>C	NP_056993.2:n.6841-117A>C
NR_052013.2:n.6689-117A>C
NR_052013.3:n.6675-117A>C
ENST00000281513.9:c.6841-117A>C	ENSP00000281513.5:n.6841-117A>C
ENST00000417461.5:c.921-117A>C	ENSP00000392421.1:n.921-117A>C
ENST00000433283.5:c.280-117A>C	ENSP00000390920.1:n.280-117A>C
ENST00000442506.5:c.3984-117A>C
ENST00000485694.1:n.1392-117A>C
ENST00000700061.1:c.4827-117A>C
ENST00000700062.1:c.4835-117A>C
ENST00000700063.1:c.1352-117A>C
ENST00000700064.1:c.2846-117A>C
XM_011510357.1:c.6712-117A>C	XP_011508659.1:n.6712-117A>C
XM_011510357.2:c.6712-117A>C	XP_011508659.1:n.6712-117A>C
XM_011510358.1:c.6712-117A>C	XP_011508660.1:n.6712-117A>C
XM_011510358.2:c.6712-117A>C	XP_011508660.1:n.6712-117A>C
XM_011510359.1:c.6202-117A>C	XP_011508661.1:n.6202-117A>C
XM_011510360.1:c.4642-117A>C	XP_011508662.1:n.4642-117A>C
XM_011510360.2:c.4642-117A>C	XP_011508662.1:n.4642-117A>C
XM_011510361.1:c.4633-117A>C	XP_011508663.1:n.4633-117A>C
XM_011510361.2:c.4633-117A>C	XP_011508663.1:n.4633-117A>C
XM_017004317.1:c.6840+11548A>C	XP_016859806.1:n.6840+11548A>C
XM_024452961.1:c.6202-117A>C	XP_024308729.1:n.6202-117A>C