Canonical Allele Identifier: CA345883817

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15358925A>G (hg19) ; chr2:g.15218801A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218801A>G , CM000664.2:g.15218801A>G	GRCh38
NC_000002.11:g.15358925A>G , CM000664.1:g.15358925A>G	GRCh37
NC_000002.10:g.15276376A>G	NCBI36
NG_032964.1:g.347548T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.4390T>C
ENST00000700062.1:c.4426+13621T>C
ENST00000700063.1:c.915T>C
ENST00000700064.1:c.2260T>C
ENST00000281513.10:c.6404T>C MANE Select	ENSP00000281513.5:p.Ile2135Thr
ENST00000281513.9:c.6404T>C	ENSP00000281513.5:p.Ile2135Thr
ENST00000417461.5:c.512+13621T>C	ENSP00000392421.1:n.512+13621T>C
ENST00000442506.5:c.3547T>C
NM_015909.3:c.6404T>C	NP_056993.2:p.Ile2135Thr
NR_052013.2:n.6280+13621T>C
XM_011510357.1:c.6275T>C	XP_011508659.1:p.Ile2092Thr
XM_011510358.1:c.6404T>C	XP_011508660.1:p.Ile2135Thr
XM_011510359.1:c.5765T>C	XP_011508661.1:p.Ile1922Thr
XM_011510360.1:c.4205T>C	XP_011508662.1:p.Ile1402Thr
XM_011510361.1:c.4196T>C	XP_011508663.1:p.Ile1399Thr
XM_011510357.2:c.6275T>C	XP_011508659.1:p.Ile2092Thr
XM_011510358.2:c.6404T>C	XP_011508660.1:p.Ile2135Thr
XM_011510360.2:c.4205T>C	XP_011508662.1:p.Ile1402Thr
XM_011510361.2:c.4196T>C	XP_011508663.1:p.Ile1399Thr
XM_017004317.1:c.6404T>C	XP_016859806.1:p.Ile2135Thr
XM_024452961.1:c.5765T>C	XP_024308729.1:p.Ile1922Thr
NM_015909.4:c.6404T>C MANE Select	NP_056993.2:p.Ile2135Thr
NR_052013.3:n.6266+13621T>C