Canonical Allele Identifier: CA2657911719

Gene: NBAS

Linked Data

• gnomAD v4: 2-15402305-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402305C>A , CM000664.2:g.15402305C>A	GRCh38
NC_000002.11:g.15542429C>A , CM000664.1:g.15542429C>A	GRCh37
NC_000002.10:g.15459880C>A	NCBI36
NG_032964.1:g.164044G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1035-4G>T
ENST00000700062.1:c.1035-4G>T
ENST00000700065.1:n.2951-4G>T
ENST00000281513.10:c.2938-4G>T MANE Select	ENSP00000281513.5:n.2938-4G>T
ENST00000281513.9:c.2938-4G>T	ENSP00000281513.5:n.2938-4G>T
ENST00000429842.1:c.230-4G>T
ENST00000441755.5:c.79-4G>T	ENSP00000396501.1:n.79-4G>T
ENST00000442506.5:c.81-4G>T
NM_015909.3:c.2938-4G>T	NP_056993.2:n.2938-4G>T
NR_052013.2:n.2982-4G>T
XM_011510357.1:c.2809-4G>T	XP_011508659.1:n.2809-4G>T
XM_011510358.1:c.2938-4G>T	XP_011508660.1:n.2938-4G>T
XM_011510359.1:c.2299-4G>T	XP_011508661.1:n.2299-4G>T
XM_011510360.1:c.739-4G>T	XP_011508662.1:n.739-4G>T
XM_011510361.1:c.730-4G>T	XP_011508663.1:n.730-4G>T
XM_011510357.2:c.2809-4G>T	XP_011508659.1:n.2809-4G>T
XM_011510358.2:c.2938-4G>T	XP_011508660.1:n.2938-4G>T
XM_011510360.2:c.739-4G>T	XP_011508662.1:n.739-4G>T
XM_011510361.2:c.730-4G>T	XP_011508663.1:n.730-4G>T
XM_017004317.1:c.2938-4G>T	XP_016859806.1:n.2938-4G>T
XM_024452961.1:c.2299-4G>T	XP_024308729.1:n.2299-4G>T
NM_015909.4:c.2938-4G>T MANE Select	NP_056993.2:n.2938-4G>T
NR_052013.3:n.2968-4G>T