Canonical Allele Identifier: CA2490796228

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218888_15218889delinsCG , CM000664.2:g.15218888_15218889delinsCG	GRCh38
NC_000002.11:g.15359012_15359013delinsCG , CM000664.1:g.15359012_15359013delinsCG	GRCh37
NC_000002.10:g.15276463_15276464delinsCG	NCBI36
NG_032964.1:g.347460_347461delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4302_4303delinsCG
ENST00000700062.1:c.4426+13533_4426+13534delinsCG
ENST00000700063.1:c.827_828delinsCG
ENST00000700064.1:c.2172_2173delinsCG
ENST00000281513.10:c.6316_6317delinsCG MANE Select	ENSP00000281513.5:p.Arg2106=
ENST00000281513.9:c.6316_6317delinsCG	ENSP00000281513.5:p.Arg2106=
ENST00000417461.5:c.512+13533_512+13534delinsCG	ENSP00000392421.1:n.512+13533_512+13534delinsCG
ENST00000442506.5:c.3459_3460delinsCG
NM_015909.3:c.6316_6317delinsCG	NP_056993.2:p.Arg2106=
NR_052013.2:n.6280+13533_6280+13534delinsCG
XM_011510357.1:c.6187_6188delinsCG	XP_011508659.1:p.Arg2063=
XM_011510358.1:c.6316_6317delinsCG	XP_011508660.1:p.Arg2106=
XM_011510359.1:c.5677_5678delinsCG	XP_011508661.1:p.Arg1893=
XM_011510360.1:c.4117_4118delinsCG	XP_011508662.1:p.Arg1373=
XM_011510361.1:c.4108_4109delinsCG	XP_011508663.1:p.Arg1370=
XM_011510357.2:c.6187_6188delinsCG	XP_011508659.1:p.Arg2063=
XM_011510358.2:c.6316_6317delinsCG	XP_011508660.1:p.Arg2106=
XM_011510360.2:c.4117_4118delinsCG	XP_011508662.1:p.Arg1373=
XM_011510361.2:c.4108_4109delinsCG	XP_011508663.1:p.Arg1370=
XM_017004317.1:c.6316_6317delinsCG	XP_016859806.1:p.Arg2106=
XM_024452961.1:c.5677_5678delinsCG	XP_024308729.1:p.Arg1893=
NM_015909.4:c.6316_6317delinsCG MANE Select	NP_056993.2:p.Arg2106=
NR_052013.3:n.6266+13533_6266+13534delinsCG