Canonical Allele Identifier: CA2657911708

Gene: NBAS

Linked Data

• gnomAD v4: 2-15402141-TAAGACTGGCATAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402142_15402154del , CM000664.2:g.15402142_15402154del	GRCh38
NC_000002.11:g.15542266_15542278del , CM000664.1:g.15542266_15542278del	GRCh37
NC_000002.10:g.15459717_15459729del	NCBI36
NG_032964.1:g.164195_164207del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1168+14_1168+26del
ENST00000700062.1:c.1168+14_1168+26del
ENST00000700065.1:n.3084+14_3084+26del
ENST00000281513.10:c.3071+14_3071+26del MANE Select	ENSP00000281513.5:n.3071+14_3071+26del
ENST00000281513.9:c.3071+14_3071+26del	ENSP00000281513.5:n.3071+14_3071+26del
ENST00000429842.1:c.363+14_363+26del
ENST00000441755.5:c.212+14_212+26del	ENSP00000396501.1:n.212+14_212+26del
ENST00000442506.5:c.214+14_214+26del
NM_015909.3:c.3071+14_3071+26del	NP_056993.2:n.3071+14_3071+26del
NR_052013.2:n.3115+14_3115+26del
XM_011510357.1:c.2942+14_2942+26del	XP_011508659.1:n.2942+14_2942+26del
XM_011510358.1:c.3071+14_3071+26del	XP_011508660.1:n.3071+14_3071+26del
XM_011510359.1:c.2432+14_2432+26del	XP_011508661.1:n.2432+14_2432+26del
XM_011510360.1:c.872+14_872+26del	XP_011508662.1:n.872+14_872+26del
XM_011510361.1:c.863+14_863+26del	XP_011508663.1:n.863+14_863+26del
XM_011510357.2:c.2942+14_2942+26del	XP_011508659.1:n.2942+14_2942+26del
XM_011510358.2:c.3071+14_3071+26del	XP_011508660.1:n.3071+14_3071+26del
XM_011510360.2:c.872+14_872+26del	XP_011508662.1:n.872+14_872+26del
XM_011510361.2:c.863+14_863+26del	XP_011508663.1:n.863+14_863+26del
XM_017004317.1:c.3071+14_3071+26del	XP_016859806.1:n.3071+14_3071+26del
XM_024452961.1:c.2432+14_2432+26del	XP_024308729.1:n.2432+14_2432+26del
NM_015909.4:c.3071+14_3071+26del MANE Select	NP_056993.2:n.3071+14_3071+26del
NR_052013.3:n.3101+14_3101+26del