Canonical Allele Identifier: CA2657912265

Gene: NBAS

Linked Data

• gnomAD v4: 2-15424603-CTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424605_15424606del , CM000664.2:g.15424605_15424606del	GRCh38
NC_000002.11:g.15564729_15564730del , CM000664.1:g.15564729_15564730del	GRCh37
NC_000002.10:g.15482180_15482181del	NCBI36
NG_032964.1:g.141744_141745del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.521-137_521-136del
ENST00000700062.1:c.521-137_521-136del
ENST00000700065.1:n.2437-137_2437-136del
ENST00000700066.1:c.1941-137_1941-136del	ENSP00000514780.1:n.1941-137_1941-136del
ENST00000281513.10:c.2424-137_2424-136del MANE Select	ENSP00000281513.5:n.2424-137_2424-136del
ENST00000281513.9:c.2424-137_2424-136del	ENSP00000281513.5:n.2424-137_2424-136del
NM_015909.3:c.2424-137_2424-136del	NP_056993.2:n.2424-137_2424-136del
NR_052013.2:n.2468-137_2468-136del
XM_011510357.1:c.2295-137_2295-136del	XP_011508659.1:n.2295-137_2295-136del
XM_011510358.1:c.2424-137_2424-136del	XP_011508660.1:n.2424-137_2424-136del
XM_011510359.1:c.1785-137_1785-136del	XP_011508661.1:n.1785-137_1785-136del
XM_011510360.1:c.225-137_225-136del	XP_011508662.1:n.225-137_225-136del
XM_011510361.1:c.216-137_216-136del	XP_011508663.1:n.216-137_216-136del
XM_011510357.2:c.2295-137_2295-136del	XP_011508659.1:n.2295-137_2295-136del
XM_011510358.2:c.2424-137_2424-136del	XP_011508660.1:n.2424-137_2424-136del
XM_011510360.2:c.225-137_225-136del	XP_011508662.1:n.225-137_225-136del
XM_011510361.2:c.216-137_216-136del	XP_011508663.1:n.216-137_216-136del
XM_017004317.1:c.2424-137_2424-136del	XP_016859806.1:n.2424-137_2424-136del
XM_024452961.1:c.1785-137_1785-136del	XP_024308729.1:n.1785-137_1785-136del
NM_015909.4:c.2424-137_2424-136del MANE Select	NP_056993.2:n.2424-137_2424-136del
NR_052013.3:n.2454-137_2454-136del