Canonical Allele Identifier: CA424866925

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15358945C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218821C>A , CM000664.2:g.15218821C>A	GRCh38
NC_000002.11:g.15358945C>A , CM000664.1:g.15358945C>A	GRCh37
NC_000002.10:g.15276396C>A	NCBI36
NG_032964.1:g.347528G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4370G>T
ENST00000700062.1:c.4426+13601G>T
ENST00000700063.1:c.895G>T
ENST00000700064.1:c.2240G>T
ENST00000281513.10:c.6384G>T MANE Select	ENSP00000281513.5:p.Val2128=
ENST00000281513.9:c.6384G>T	ENSP00000281513.5:p.Val2128=
ENST00000417461.5:c.512+13601G>T	ENSP00000392421.1:n.512+13601G>T
ENST00000442506.5:c.3527G>T
NM_015909.3:c.6384G>T	NP_056993.2:p.Val2128=
NR_052013.2:n.6280+13601G>T
XM_011510357.1:c.6255G>T	XP_011508659.1:p.Val2085=
XM_011510358.1:c.6384G>T	XP_011508660.1:p.Val2128=
XM_011510359.1:c.5745G>T	XP_011508661.1:p.Val1915=
XM_011510360.1:c.4185G>T	XP_011508662.1:p.Val1395=
XM_011510361.1:c.4176G>T	XP_011508663.1:p.Val1392=
XM_011510357.2:c.6255G>T	XP_011508659.1:p.Val2085=
XM_011510358.2:c.6384G>T	XP_011508660.1:p.Val2128=
XM_011510360.2:c.4185G>T	XP_011508662.1:p.Val1395=
XM_011510361.2:c.4176G>T	XP_011508663.1:p.Val1392=
XM_017004317.1:c.6384G>T	XP_016859806.1:p.Val2128=
XM_024452961.1:c.5745G>T	XP_024308729.1:p.Val1915=
NM_015909.4:c.6384G>T MANE Select	NP_056993.2:p.Val2128=
NR_052013.3:n.6266+13601G>T