Canonical Allele Identifier: CA2576680253

Gene: NBAS

Linked Data

• gnomAD v4: 2-15219057-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15219057C>T , CM000664.2:g.15219057C>T	GRCh38
NC_000002.11:g.15359181C>T , CM000664.1:g.15359181C>T	GRCh37
NC_000002.10:g.15276632C>T	NCBI36
NG_032964.1:g.347292G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4223-89G>A
ENST00000700062.1:c.4426+13365G>A
ENST00000700063.1:c.748-89G>A
ENST00000700064.1:c.2093-89G>A
ENST00000281513.10:c.6237-89G>A MANE Select	ENSP00000281513.5:n.6237-89G>A
ENST00000281513.9:c.6237-89G>A	ENSP00000281513.5:n.6237-89G>A
ENST00000417461.5:c.512+13365G>A	ENSP00000392421.1:n.512+13365G>A
ENST00000442506.5:c.3380-89G>A
NM_015909.3:c.6237-89G>A	NP_056993.2:n.6237-89G>A
NR_052013.2:n.6280+13365G>A
XM_011510357.1:c.6108-89G>A	XP_011508659.1:n.6108-89G>A
XM_011510358.1:c.6237-89G>A	XP_011508660.1:n.6237-89G>A
XM_011510359.1:c.5598-89G>A	XP_011508661.1:n.5598-89G>A
XM_011510360.1:c.4038-89G>A	XP_011508662.1:n.4038-89G>A
XM_011510361.1:c.4029-89G>A	XP_011508663.1:n.4029-89G>A
XM_011510357.2:c.6108-89G>A	XP_011508659.1:n.6108-89G>A
XM_011510358.2:c.6237-89G>A	XP_011508660.1:n.6237-89G>A
XM_011510360.2:c.4038-89G>A	XP_011508662.1:n.4038-89G>A
XM_011510361.2:c.4029-89G>A	XP_011508663.1:n.4029-89G>A
XM_017004317.1:c.6237-89G>A	XP_016859806.1:n.6237-89G>A
XM_024452961.1:c.5598-89G>A	XP_024308729.1:n.5598-89G>A
NM_015909.4:c.6237-89G>A MANE Select	NP_056993.2:n.6237-89G>A
NR_052013.3:n.6266+13365G>A