Canonical Allele Identifier: CA424870584

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15564538C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424414C>T , CM000664.2:g.15424414C>T	GRCh38
NC_000002.11:g.15564538C>T , CM000664.1:g.15564538C>T	GRCh37
NC_000002.10:g.15481989C>T	NCBI36
NG_032964.1:g.141935G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.575G>A
ENST00000700062.1:c.575G>A
ENST00000700065.1:n.2491G>A
ENST00000700066.1:c.1995G>A	ENSP00000514780.1:p.Gln665=
ENST00000281513.10:c.2478G>A MANE Select	ENSP00000281513.5:p.Gln826=
ENST00000281513.9:c.2478G>A	ENSP00000281513.5:p.Gln826=
NM_015909.3:c.2478G>A	NP_056993.2:p.Gln826=
NR_052013.2:n.2522G>A
XM_011510357.1:c.2349G>A	XP_011508659.1:p.Gln783=
XM_011510358.1:c.2478G>A	XP_011508660.1:p.Gln826=
XM_011510359.1:c.1839G>A	XP_011508661.1:p.Gln613=
XM_011510360.1:c.279G>A	XP_011508662.1:p.Gln93=
XM_011510361.1:c.270G>A	XP_011508663.1:p.Gln90=
XM_011510357.2:c.2349G>A	XP_011508659.1:p.Gln783=
XM_011510358.2:c.2478G>A	XP_011508660.1:p.Gln826=
XM_011510360.2:c.279G>A	XP_011508662.1:p.Gln93=
XM_011510361.2:c.270G>A	XP_011508663.1:p.Gln90=
XM_017004317.1:c.2478G>A	XP_016859806.1:p.Gln826=
XM_024452961.1:c.1839G>A	XP_024308729.1:p.Gln613=
NM_015909.4:c.2478G>A MANE Select	NP_056993.2:p.Gln826=
NR_052013.3:n.2508G>A