Canonical Allele Identifier: CA345890277

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15564576T>A (hg19) ; chr2:g.15424452T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424452T>A , CM000664.2:g.15424452T>A	GRCh38
NC_000002.11:g.15564576T>A , CM000664.1:g.15564576T>A	GRCh37
NC_000002.10:g.15482027T>A	NCBI36
NG_032964.1:g.141897A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.537A>T
ENST00000700062.1:c.537A>T
ENST00000700065.1:n.2453A>T
ENST00000700066.1:c.1957A>T	ENSP00000514780.1:p.Asn653Tyr
ENST00000281513.10:c.2440A>T MANE Select	ENSP00000281513.5:p.Asn814Tyr
ENST00000281513.9:c.2440A>T	ENSP00000281513.5:p.Asn814Tyr
NM_015909.3:c.2440A>T	NP_056993.2:p.Asn814Tyr
NR_052013.2:n.2484A>T
XM_011510357.1:c.2311A>T	XP_011508659.1:p.Asn771Tyr
XM_011510358.1:c.2440A>T	XP_011508660.1:p.Asn814Tyr
XM_011510359.1:c.1801A>T	XP_011508661.1:p.Asn601Tyr
XM_011510360.1:c.241A>T	XP_011508662.1:p.Asn81Tyr
XM_011510361.1:c.232A>T	XP_011508663.1:p.Asn78Tyr
XM_011510357.2:c.2311A>T	XP_011508659.1:p.Asn771Tyr
XM_011510358.2:c.2440A>T	XP_011508660.1:p.Asn814Tyr
XM_011510360.2:c.241A>T	XP_011508662.1:p.Asn81Tyr
XM_011510361.2:c.232A>T	XP_011508663.1:p.Asn78Tyr
XM_017004317.1:c.2440A>T	XP_016859806.1:p.Asn814Tyr
XM_024452961.1:c.1801A>T	XP_024308729.1:p.Asn601Tyr
NM_015909.4:c.2440A>T MANE Select	NP_056993.2:p.Asn814Tyr
NR_052013.3:n.2470A>T