Canonical Allele Identifier: CA345883897

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15358937C>G (hg19) ; chr2:g.15218813C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218813C>G , CM000664.2:g.15218813C>G	GRCh38
NC_000002.11:g.15358937C>G , CM000664.1:g.15358937C>G	GRCh37
NC_000002.10:g.15276388C>G	NCBI36
NG_032964.1:g.347536G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4378G>C
ENST00000700062.1:c.4426+13609G>C
ENST00000700063.1:c.903G>C
ENST00000700064.1:c.2248G>C
ENST00000281513.10:c.6392G>C MANE Select	ENSP00000281513.5:p.Arg2131Thr
ENST00000281513.9:c.6392G>C	ENSP00000281513.5:p.Arg2131Thr
ENST00000417461.5:c.512+13609G>C	ENSP00000392421.1:n.512+13609G>C
ENST00000442506.5:c.3535G>C
NM_015909.3:c.6392G>C	NP_056993.2:p.Arg2131Thr
NR_052013.2:n.6280+13609G>C
XM_011510357.1:c.6263G>C	XP_011508659.1:p.Arg2088Thr
XM_011510358.1:c.6392G>C	XP_011508660.1:p.Arg2131Thr
XM_011510359.1:c.5753G>C	XP_011508661.1:p.Arg1918Thr
XM_011510360.1:c.4193G>C	XP_011508662.1:p.Arg1398Thr
XM_011510361.1:c.4184G>C	XP_011508663.1:p.Arg1395Thr
XM_011510357.2:c.6263G>C	XP_011508659.1:p.Arg2088Thr
XM_011510358.2:c.6392G>C	XP_011508660.1:p.Arg2131Thr
XM_011510360.2:c.4193G>C	XP_011508662.1:p.Arg1398Thr
XM_011510361.2:c.4184G>C	XP_011508663.1:p.Arg1395Thr
XM_017004317.1:c.6392G>C	XP_016859806.1:p.Arg2131Thr
XM_024452961.1:c.5753G>C	XP_024308729.1:p.Arg1918Thr
NM_015909.4:c.6392G>C MANE Select	NP_056993.2:p.Arg2131Thr
NR_052013.3:n.6266+13609G>C