Canonical Allele Identifier: CA345883841

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15358929C>A (hg19) ; chr2:g.15218805C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218805C>A , CM000664.2:g.15218805C>A	GRCh38
NC_000002.11:g.15358929C>A , CM000664.1:g.15358929C>A	GRCh37
NC_000002.10:g.15276380C>A	NCBI36
NG_032964.1:g.347544G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.4386G>T
ENST00000700062.1:c.4426+13617G>T
ENST00000700063.1:c.911G>T
ENST00000700064.1:c.2256G>T
ENST00000281513.10:c.6400G>T MANE Select	ENSP00000281513.5:p.Ala2134Ser
ENST00000281513.9:c.6400G>T	ENSP00000281513.5:p.Ala2134Ser
ENST00000417461.5:c.512+13617G>T	ENSP00000392421.1:n.512+13617G>T
ENST00000442506.5:c.3543G>T
NM_015909.3:c.6400G>T	NP_056993.2:p.Ala2134Ser
NR_052013.2:n.6280+13617G>T
XM_011510357.1:c.6271G>T	XP_011508659.1:p.Ala2091Ser
XM_011510358.1:c.6400G>T	XP_011508660.1:p.Ala2134Ser
XM_011510359.1:c.5761G>T	XP_011508661.1:p.Ala1921Ser
XM_011510360.1:c.4201G>T	XP_011508662.1:p.Ala1401Ser
XM_011510361.1:c.4192G>T	XP_011508663.1:p.Ala1398Ser
XM_011510357.2:c.6271G>T	XP_011508659.1:p.Ala2091Ser
XM_011510358.2:c.6400G>T	XP_011508660.1:p.Ala2134Ser
XM_011510360.2:c.4201G>T	XP_011508662.1:p.Ala1401Ser
XM_011510361.2:c.4192G>T	XP_011508663.1:p.Ala1398Ser
XM_017004317.1:c.6400G>T	XP_016859806.1:p.Ala2134Ser
XM_024452961.1:c.5761G>T	XP_024308729.1:p.Ala1921Ser
NM_015909.4:c.6400G>T MANE Select	NP_056993.2:p.Ala2134Ser
NR_052013.3:n.6266+13617G>T