Canonical Allele Identifier: CA531314719

Gene: NBAS

Linked Data

• dbSNP Id: rs1174472808
• gnomAD v2: 2-15359111-AG-A
• gnomAD v4: 2-15218987-AG-A
• MyVariant Identifiers: chr2:g.15359112del (hg19) ; chr2:g.15218988del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218989del , CM000664.2:g.15218989del	GRCh38
NC_000002.11:g.15359113del , CM000664.1:g.15359113del	GRCh37
NC_000002.10:g.15276564del	NCBI36
NG_032964.1:g.347361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4223-20del
ENST00000700062.1:c.4426+13434del
ENST00000700063.1:c.748-20del
ENST00000700064.1:c.2093-20del
ENST00000281513.10:c.6237-20del MANE Select	ENSP00000281513.5:n.6237-20del
ENST00000281513.9:c.6237-20del	ENSP00000281513.5:n.6237-20del
ENST00000417461.5:c.512+13434del	ENSP00000392421.1:n.512+13434del
ENST00000442506.5:c.3380-20del
NM_015909.3:c.6237-20del	NP_056993.2:n.6237-20del
NR_052013.2:n.6280+13434del
XM_011510357.1:c.6108-20del	XP_011508659.1:n.6108-20del
XM_011510358.1:c.6237-20del	XP_011508660.1:n.6237-20del
XM_011510359.1:c.5598-20del	XP_011508661.1:n.5598-20del
XM_011510360.1:c.4038-20del	XP_011508662.1:n.4038-20del
XM_011510361.1:c.4029-20del	XP_011508663.1:n.4029-20del
XM_011510357.2:c.6108-20del	XP_011508659.1:n.6108-20del
XM_011510358.2:c.6237-20del	XP_011508660.1:n.6237-20del
XM_011510360.2:c.4038-20del	XP_011508662.1:n.4038-20del
XM_011510361.2:c.4029-20del	XP_011508663.1:n.4029-20del
XM_017004317.1:c.6237-20del	XP_016859806.1:n.6237-20del
XM_024452961.1:c.5598-20del	XP_024308729.1:n.5598-20del
NM_015909.4:c.6237-20del MANE Select	NP_056993.2:n.6237-20del
NR_052013.3:n.6266+13434del