Canonical Allele Identifier: CA531015696

Gene: NBAS

Linked Data

• dbSNP Id: rs1169673626
• gnomAD v2: 2-15358548-G-GT
• gnomAD v3: 2-15218424-G-GT
• gnomAD v4: 2-15218424-G-GT
• MyVariant Identifiers: chr2:g.15358549_15358550insT (hg19) ; chr2:g.15218425_15218426insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218431dup , CM000664.2:g.15218431dup	GRCh38
NC_000002.11:g.15358555dup , CM000664.1:g.15358555dup	GRCh37
NC_000002.10:g.15276006dup	NCBI36
NG_032964.1:g.347924dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4418+348dup
ENST00000700062.1:c.4426+13997dup
ENST00000700063.1:c.943+348dup
ENST00000700064.1:c.2288+348dup
ENST00000281513.10:c.6432+348dup MANE Select	ENSP00000281513.5:n.6432+348dup
ENST00000281513.9:c.6432+348dup	ENSP00000281513.5:n.6432+348dup
ENST00000417461.5:c.512+13997dup	ENSP00000392421.1:n.512+13997dup
ENST00000442506.5:c.3575+348dup
NM_015909.3:c.6432+348dup	NP_056993.2:n.6432+348dup
NR_052013.2:n.6280+13997dup
XM_011510357.1:c.6303+348dup	XP_011508659.1:n.6303+348dup
XM_011510358.1:c.6432+348dup	XP_011508660.1:n.6432+348dup
XM_011510359.1:c.5793+348dup	XP_011508661.1:n.5793+348dup
XM_011510360.1:c.4233+348dup	XP_011508662.1:n.4233+348dup
XM_011510361.1:c.4224+348dup	XP_011508663.1:n.4224+348dup
XM_011510357.2:c.6303+348dup	XP_011508659.1:n.6303+348dup
XM_011510358.2:c.6432+348dup	XP_011508660.1:n.6432+348dup
XM_011510360.2:c.4233+348dup	XP_011508662.1:n.4233+348dup
XM_011510361.2:c.4224+348dup	XP_011508663.1:n.4224+348dup
XM_017004317.1:c.6432+348dup	XP_016859806.1:n.6432+348dup
XM_024452961.1:c.5793+348dup	XP_024308729.1:n.5793+348dup
NM_015909.4:c.6432+348dup MANE Select	NP_056993.2:n.6432+348dup
NR_052013.3:n.6266+13997dup