Canonical Allele Identifier: CA3038409827

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15308172G>T , CM000664.2:g.15308172G>T	GRCh38
NC_000002.11:g.15448296G>T , CM000664.1:g.15448296G>T	GRCh37
NC_000002.10:g.15365747G>T	NCBI36
NG_032964.1:g.258177C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015909.4:c.4797+44C>A MANE Select	NP_056993.2:n.4797+44C>A
ENST00000281513.10:c.4797+44C>A MANE Select	ENSP00000281513.5:n.4797+44C>A
NM_015909.3:c.4797+44C>A	NP_056993.2:n.4797+44C>A
NR_052013.2:n.4841+44C>A
NR_052013.3:n.4827+44C>A
ENST00000281513.9:c.4797+44C>A	ENSP00000281513.5:n.4797+44C>A
ENST00000442506.5:c.1940+44C>A
ENST00000700061.1:c.2894+44C>A
ENST00000700062.1:c.2987+44C>A
ENST00000700064.1:c.653+44C>A
ENST00000700065.1:n.4810+44C>A
XM_011510357.1:c.4668+44C>A	XP_011508659.1:n.4668+44C>A
XM_011510357.2:c.4668+44C>A	XP_011508659.1:n.4668+44C>A
XM_011510358.1:c.4797+44C>A	XP_011508660.1:n.4797+44C>A
XM_011510358.2:c.4797+44C>A	XP_011508660.1:n.4797+44C>A
XM_011510359.1:c.4158+44C>A	XP_011508661.1:n.4158+44C>A
XM_011510360.1:c.2598+44C>A	XP_011508662.1:n.2598+44C>A
XM_011510360.2:c.2598+44C>A	XP_011508662.1:n.2598+44C>A
XM_011510361.1:c.2589+44C>A	XP_011508663.1:n.2589+44C>A
XM_011510361.2:c.2589+44C>A	XP_011508663.1:n.2589+44C>A
XM_017004317.1:c.4797+44C>A	XP_016859806.1:n.4797+44C>A
XM_024452961.1:c.4158+44C>A	XP_024308729.1:n.4158+44C>A