Canonical Allele Identifier: CA2490889368

Gene: NBAS

Linked Data

• ClinVar Variation Id: 1671662
• ClinVar RCV Id: RCV002199128
• dbSNP Id: rs1572828888
• gnomAD v4: 2-15424479-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424479C>T , CM000664.2:g.15424479C>T	GRCh38
NC_000002.11:g.15564603C>T , CM000664.1:g.15564603C>T	GRCh37
NC_000002.10:g.15482054C>T	NCBI36
NG_032964.1:g.141870G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.521-11G>A
ENST00000700062.1:c.521-11G>A
ENST00000700065.1:n.2437-11G>A
ENST00000700066.1:c.1941-11G>A	ENSP00000514780.1:n.1941-11G>A
ENST00000281513.10:c.2424-11G>A MANE Select	ENSP00000281513.5:n.2424-11G>A
ENST00000281513.9:c.2424-11G>A	ENSP00000281513.5:n.2424-11G>A
NM_015909.3:c.2424-11G>A	NP_056993.2:n.2424-11G>A
NR_052013.2:n.2468-11G>A
XM_011510357.1:c.2295-11G>A	XP_011508659.1:n.2295-11G>A
XM_011510358.1:c.2424-11G>A	XP_011508660.1:n.2424-11G>A
XM_011510359.1:c.1785-11G>A	XP_011508661.1:n.1785-11G>A
XM_011510360.1:c.225-11G>A	XP_011508662.1:n.225-11G>A
XM_011510361.1:c.216-11G>A	XP_011508663.1:n.216-11G>A
XM_011510357.2:c.2295-11G>A	XP_011508659.1:n.2295-11G>A
XM_011510358.2:c.2424-11G>A	XP_011508660.1:n.2424-11G>A
XM_011510360.2:c.225-11G>A	XP_011508662.1:n.225-11G>A
XM_011510361.2:c.216-11G>A	XP_011508663.1:n.216-11G>A
XM_017004317.1:c.2424-11G>A	XP_016859806.1:n.2424-11G>A
XM_024452961.1:c.1785-11G>A	XP_024308729.1:n.1785-11G>A
NM_015909.4:c.2424-11G>A MANE Select	NP_056993.2:n.2424-11G>A
NR_052013.3:n.2454-11G>A