Canonical Allele Identifier: CA42632245

Gene: NBAS

Linked Data

• dbSNP Id: rs895885162
• MyVariant Identifiers: chr2:g.15564202C>T (hg19) ; chr2:g.15424078C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424078C>T , CM000664.2:g.15424078C>T	GRCh38
NC_000002.11:g.15564202C>T , CM000664.1:g.15564202C>T	GRCh37
NC_000002.10:g.15481653C>T	NCBI36
NG_032964.1:g.142271G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.674+237G>A
ENST00000700062.1:c.674+237G>A
ENST00000700065.1:n.2590+237G>A
ENST00000700066.1:c.2094+237G>A	ENSP00000514780.1:n.2094+237G>A
ENST00000281513.10:c.2577+237G>A MANE Select	ENSP00000281513.5:n.2577+237G>A
ENST00000281513.9:c.2577+237G>A	ENSP00000281513.5:n.2577+237G>A
ENST00000441755.5:c.78+237G>A	ENSP00000396501.1:n.78+237G>A
ENST00000442506.5:c.80+237G>A
NM_015909.3:c.2577+237G>A	NP_056993.2:n.2577+237G>A
NR_052013.2:n.2621+237G>A
XM_011510357.1:c.2448+237G>A	XP_011508659.1:n.2448+237G>A
XM_011510358.1:c.2577+237G>A	XP_011508660.1:n.2577+237G>A
XM_011510359.1:c.1938+237G>A	XP_011508661.1:n.1938+237G>A
XM_011510360.1:c.378+237G>A	XP_011508662.1:n.378+237G>A
XM_011510361.1:c.369+237G>A	XP_011508663.1:n.369+237G>A
XM_011510357.2:c.2448+237G>A	XP_011508659.1:n.2448+237G>A
XM_011510358.2:c.2577+237G>A	XP_011508660.1:n.2577+237G>A
XM_011510360.2:c.378+237G>A	XP_011508662.1:n.378+237G>A
XM_011510361.2:c.369+237G>A	XP_011508663.1:n.369+237G>A
XM_017004317.1:c.2577+237G>A	XP_016859806.1:n.2577+237G>A
XM_024452961.1:c.1938+237G>A	XP_024308729.1:n.1938+237G>A
NM_015909.4:c.2577+237G>A MANE Select	NP_056993.2:n.2577+237G>A
NR_052013.3:n.2607+237G>A