Canonical Allele Identifier: CA345889002

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15564447C>A (hg19) ; chr2:g.15424323C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424323C>A , CM000664.2:g.15424323C>A	GRCh38
NC_000002.11:g.15564447C>A , CM000664.1:g.15564447C>A	GRCh37
NC_000002.10:g.15481898C>A	NCBI36
NG_032964.1:g.142026G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.666G>T
ENST00000700062.1:c.666G>T
ENST00000700065.1:n.2582G>T
ENST00000700066.1:c.2086G>T	ENSP00000514780.1:p.Ala696Ser
ENST00000281513.10:c.2569G>T MANE Select	ENSP00000281513.5:p.Ala857Ser
ENST00000281513.9:c.2569G>T	ENSP00000281513.5:p.Ala857Ser
ENST00000441755.5:c.70G>T	ENSP00000396501.1:p.Ala24Ser
ENST00000442506.5:c.72G>T
NM_015909.3:c.2569G>T	NP_056993.2:p.Ala857Ser
NR_052013.2:n.2613G>T
XM_011510357.1:c.2440G>T	XP_011508659.1:p.Ala814Ser
XM_011510358.1:c.2569G>T	XP_011508660.1:p.Ala857Ser
XM_011510359.1:c.1930G>T	XP_011508661.1:p.Ala644Ser
XM_011510360.1:c.370G>T	XP_011508662.1:p.Ala124Ser
XM_011510361.1:c.361G>T	XP_011508663.1:p.Ala121Ser
XM_011510357.2:c.2440G>T	XP_011508659.1:p.Ala814Ser
XM_011510358.2:c.2569G>T	XP_011508660.1:p.Ala857Ser
XM_011510360.2:c.370G>T	XP_011508662.1:p.Ala124Ser
XM_011510361.2:c.361G>T	XP_011508663.1:p.Ala121Ser
XM_017004317.1:c.2569G>T	XP_016859806.1:p.Ala857Ser
XM_024452961.1:c.1930G>T	XP_024308729.1:p.Ala644Ser
NM_015909.4:c.2569G>T MANE Select	NP_056993.2:p.Ala857Ser
NR_052013.3:n.2599G>T