Canonical Allele Identifier: CA345882285

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15542394T>A (hg19) ; chr2:g.15402270T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402270T>A , CM000664.2:g.15402270T>A	GRCh38
NC_000002.11:g.15542394T>A , CM000664.1:g.15542394T>A	GRCh37
NC_000002.10:g.15459845T>A	NCBI36
NG_032964.1:g.164079A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1066A>T
ENST00000700062.1:c.1066A>T
ENST00000700065.1:n.2982A>T
ENST00000281513.10:c.2969A>T MANE Select	ENSP00000281513.5:p.Gln990Leu
ENST00000281513.9:c.2969A>T	ENSP00000281513.5:p.Gln990Leu
ENST00000429842.1:c.261A>T
ENST00000441755.5:c.110A>T	ENSP00000396501.1:p.Gln37Leu
ENST00000442506.5:c.112A>T
NM_015909.3:c.2969A>T	NP_056993.2:p.Gln990Leu
NR_052013.2:n.3013A>T
XM_011510357.1:c.2840A>T	XP_011508659.1:p.Gln947Leu
XM_011510358.1:c.2969A>T	XP_011508660.1:p.Gln990Leu
XM_011510359.1:c.2330A>T	XP_011508661.1:p.Gln777Leu
XM_011510360.1:c.770A>T	XP_011508662.1:p.Gln257Leu
XM_011510361.1:c.761A>T	XP_011508663.1:p.Gln254Leu
XM_011510357.2:c.2840A>T	XP_011508659.1:p.Gln947Leu
XM_011510358.2:c.2969A>T	XP_011508660.1:p.Gln990Leu
XM_011510360.2:c.770A>T	XP_011508662.1:p.Gln257Leu
XM_011510361.2:c.761A>T	XP_011508663.1:p.Gln254Leu
XM_017004317.1:c.2969A>T	XP_016859806.1:p.Gln990Leu
XM_024452961.1:c.2330A>T	XP_024308729.1:p.Gln777Leu
NM_015909.4:c.2969A>T MANE Select	NP_056993.2:p.Gln990Leu
NR_052013.3:n.2999A>T