Canonical Allele Identifier: CA345883823

Gene: NBAS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.4390T>A
ENST00000700062.1:c.4426+13621T>A
ENST00000700063.1:c.915T>A
ENST00000700064.1:c.2260T>A
ENST00000281513.10:c.6404T>A MANE Select	ENSP00000281513.5:p.Ile2135Asn
ENST00000281513.9:c.6404T>A	ENSP00000281513.5:p.Ile2135Asn
ENST00000417461.5:c.512+13621T>A	ENSP00000392421.1:n.512+13621T>A
ENST00000442506.5:c.3547T>A
NM_015909.3:c.6404T>A	NP_056993.2:p.Ile2135Asn
NR_052013.2:n.6280+13621T>A
XM_011510357.1:c.6275T>A	XP_011508659.1:p.Ile2092Asn
XM_011510358.1:c.6404T>A	XP_011508660.1:p.Ile2135Asn
XM_011510359.1:c.5765T>A	XP_011508661.1:p.Ile1922Asn
XM_011510360.1:c.4205T>A	XP_011508662.1:p.Ile1402Asn
XM_011510361.1:c.4196T>A	XP_011508663.1:p.Ile1399Asn
XM_011510357.2:c.6275T>A	XP_011508659.1:p.Ile2092Asn
XM_011510358.2:c.6404T>A	XP_011508660.1:p.Ile2135Asn
XM_011510360.2:c.4205T>A	XP_011508662.1:p.Ile1402Asn
XM_011510361.2:c.4196T>A	XP_011508663.1:p.Ile1399Asn
XM_017004317.1:c.6404T>A	XP_016859806.1:p.Ile2135Asn
XM_024452961.1:c.5765T>A	XP_024308729.1:p.Ile1922Asn
NM_015909.4:c.6404T>A MANE Select	NP_056993.2:p.Ile2135Asn
NR_052013.3:n.6266+13621T>A