Canonical Allele Identifier: CA2490796022

Gene: NBAS

Linked Data

• dbSNP Id: rs1666752828

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218458_15218459insA , CM000664.2:g.15218458_15218459insA	GRCh38
NC_000002.11:g.15358582_15358583insA , CM000664.1:g.15358582_15358583insA	GRCh37
NC_000002.10:g.15276033_15276034insA	NCBI36
NG_032964.1:g.347890_347891insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4418+314_4418+315insT
ENST00000700062.1:c.4426+13963_4426+13964insT
ENST00000700063.1:c.943+314_943+315insT
ENST00000700064.1:c.2288+314_2288+315insT
ENST00000281513.10:c.6432+314_6432+315insT MANE Select	ENSP00000281513.5:n.6432+314_6432+315insT
ENST00000281513.9:c.6432+314_6432+315insT	ENSP00000281513.5:n.6432+314_6432+315insT
ENST00000417461.5:c.512+13963_512+13964insT	ENSP00000392421.1:n.512+13963_512+13964insT
ENST00000442506.5:c.3575+314_3575+315insT
NM_015909.3:c.6432+314_6432+315insT	NP_056993.2:n.6432+314_6432+315insT
NR_052013.2:n.6280+13963_6280+13964insT
XM_011510357.1:c.6303+314_6303+315insT	XP_011508659.1:n.6303+314_6303+315insT
XM_011510358.1:c.6432+314_6432+315insT	XP_011508660.1:n.6432+314_6432+315insT
XM_011510359.1:c.5793+314_5793+315insT	XP_011508661.1:n.5793+314_5793+315insT
XM_011510360.1:c.4233+314_4233+315insT	XP_011508662.1:n.4233+314_4233+315insT
XM_011510361.1:c.4224+314_4224+315insT	XP_011508663.1:n.4224+314_4224+315insT
XM_011510357.2:c.6303+314_6303+315insT	XP_011508659.1:n.6303+314_6303+315insT
XM_011510358.2:c.6432+314_6432+315insT	XP_011508660.1:n.6432+314_6432+315insT
XM_011510360.2:c.4233+314_4233+315insT	XP_011508662.1:n.4233+314_4233+315insT
XM_011510361.2:c.4224+314_4224+315insT	XP_011508663.1:n.4224+314_4224+315insT
XM_017004317.1:c.6432+314_6432+315insT	XP_016859806.1:n.6432+314_6432+315insT
XM_024452961.1:c.5793+314_5793+315insT	XP_024308729.1:n.5793+314_5793+315insT
NM_015909.4:c.6432+314_6432+315insT MANE Select	NP_056993.2:n.6432+314_6432+315insT
NR_052013.3:n.6266+13963_6266+13964insT