Canonical Allele Identifier: CA2657912143

Gene: NBAS

Linked Data

• gnomAD v4: 2-15424244-G-GTGTACT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424245_15424250dup , CM000664.2:g.15424245_15424250dup	GRCh38
NC_000002.11:g.15564369_15564374dup , CM000664.1:g.15564369_15564374dup	GRCh37
NC_000002.10:g.15481820_15481825dup	NCBI36
NG_032964.1:g.142099_142104dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.674+65_674+70dup
ENST00000700062.1:c.674+65_674+70dup
ENST00000700065.1:n.2590+65_2590+70dup
ENST00000700066.1:c.2094+65_2094+70dup	ENSP00000514780.1:n.2094+65_2094+70dup
ENST00000281513.10:c.2577+65_2577+70dup MANE Select	ENSP00000281513.5:n.2577+65_2577+70dup
ENST00000281513.9:c.2577+65_2577+70dup	ENSP00000281513.5:n.2577+65_2577+70dup
ENST00000441755.5:c.78+65_78+70dup	ENSP00000396501.1:n.78+65_78+70dup
ENST00000442506.5:c.80+65_80+70dup
NM_015909.3:c.2577+65_2577+70dup	NP_056993.2:n.2577+65_2577+70dup
NR_052013.2:n.2621+65_2621+70dup
XM_011510357.1:c.2448+65_2448+70dup	XP_011508659.1:n.2448+65_2448+70dup
XM_011510358.1:c.2577+65_2577+70dup	XP_011508660.1:n.2577+65_2577+70dup
XM_011510359.1:c.1938+65_1938+70dup	XP_011508661.1:n.1938+65_1938+70dup
XM_011510360.1:c.378+65_378+70dup	XP_011508662.1:n.378+65_378+70dup
XM_011510361.1:c.369+65_369+70dup	XP_011508663.1:n.369+65_369+70dup
XM_011510357.2:c.2448+65_2448+70dup	XP_011508659.1:n.2448+65_2448+70dup
XM_011510358.2:c.2577+65_2577+70dup	XP_011508660.1:n.2577+65_2577+70dup
XM_011510360.2:c.378+65_378+70dup	XP_011508662.1:n.378+65_378+70dup
XM_011510361.2:c.369+65_369+70dup	XP_011508663.1:n.369+65_369+70dup
XM_017004317.1:c.2577+65_2577+70dup	XP_016859806.1:n.2577+65_2577+70dup
XM_024452961.1:c.1938+65_1938+70dup	XP_024308729.1:n.1938+65_1938+70dup
NM_015909.4:c.2577+65_2577+70dup MANE Select	NP_056993.2:n.2577+65_2577+70dup
NR_052013.3:n.2607+65_2607+70dup