Canonical Allele Identifier: CA2490796211

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218855A= , CM000664.2:g.15218855A=	GRCh38
NC_000002.11:g.15358979A= , CM000664.1:g.15358979A=	GRCh37
NC_000002.10:g.15276430A=	NCBI36
NG_032964.1:g.347494T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4336T=
ENST00000700062.1:c.4426+13567T=
ENST00000700063.1:c.861T=
ENST00000700064.1:c.2206T=
ENST00000281513.10:c.6350T= MANE Select	ENSP00000281513.5:p.Phe2117=
ENST00000281513.9:c.6350T=	ENSP00000281513.5:p.Phe2117=
ENST00000417461.5:c.512+13567T=	ENSP00000392421.1:n.512+13567T=
ENST00000442506.5:c.3493T=
NM_015909.3:c.6350T=	NP_056993.2:p.Phe2117=
NR_052013.2:n.6280+13567T=
XM_011510357.1:c.6221T=	XP_011508659.1:p.Phe2074=
XM_011510358.1:c.6350T=	XP_011508660.1:p.Phe2117=
XM_011510359.1:c.5711T=	XP_011508661.1:p.Phe1904=
XM_011510360.1:c.4151T=	XP_011508662.1:p.Phe1384=
XM_011510361.1:c.4142T=	XP_011508663.1:p.Phe1381=
XM_011510357.2:c.6221T=	XP_011508659.1:p.Phe2074=
XM_011510358.2:c.6350T=	XP_011508660.1:p.Phe2117=
XM_011510360.2:c.4151T=	XP_011508662.1:p.Phe1384=
XM_011510361.2:c.4142T=	XP_011508663.1:p.Phe1381=
XM_017004317.1:c.6350T=	XP_016859806.1:p.Phe2117=
XM_024452961.1:c.5711T=	XP_024308729.1:p.Phe1904=
NM_015909.4:c.6350T= MANE Select	NP_056993.2:p.Phe2117=
NR_052013.3:n.6266+13567T=