Canonical Allele Identifier: CA424870593

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15564541T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424417T>G , CM000664.2:g.15424417T>G	GRCh38
NC_000002.11:g.15564541T>G , CM000664.1:g.15564541T>G	GRCh37
NC_000002.10:g.15481992T>G	NCBI36
NG_032964.1:g.141932A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.572A>C
ENST00000700062.1:c.572A>C
ENST00000700065.1:n.2488A>C
ENST00000700066.1:c.1992A>C	ENSP00000514780.1:p.Ala664=
ENST00000281513.10:c.2475A>C MANE Select	ENSP00000281513.5:p.Ala825=
ENST00000281513.9:c.2475A>C	ENSP00000281513.5:p.Ala825=
NM_015909.3:c.2475A>C	NP_056993.2:p.Ala825=
NR_052013.2:n.2519A>C
XM_011510357.1:c.2346A>C	XP_011508659.1:p.Ala782=
XM_011510358.1:c.2475A>C	XP_011508660.1:p.Ala825=
XM_011510359.1:c.1836A>C	XP_011508661.1:p.Ala612=
XM_011510360.1:c.276A>C	XP_011508662.1:p.Ala92=
XM_011510361.1:c.267A>C	XP_011508663.1:p.Ala89=
XM_011510357.2:c.2346A>C	XP_011508659.1:p.Ala782=
XM_011510358.2:c.2475A>C	XP_011508660.1:p.Ala825=
XM_011510360.2:c.276A>C	XP_011508662.1:p.Ala92=
XM_011510361.2:c.267A>C	XP_011508663.1:p.Ala89=
XM_017004317.1:c.2475A>C	XP_016859806.1:p.Ala825=
XM_024452961.1:c.1836A>C	XP_024308729.1:p.Ala612=
NM_015909.4:c.2475A>C MANE Select	NP_056993.2:p.Ala825=
NR_052013.3:n.2505A>C