Canonical Allele Identifier: CA2490889390

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15424519_15424521delinsCAT , CM000664.2:g.15424519_15424521delinsCAT	GRCh38
NC_000002.11:g.15564643_15564645delinsCAT , CM000664.1:g.15564643_15564645delinsCAT	GRCh37
NC_000002.10:g.15482094_15482096delinsCAT	NCBI36
NG_032964.1:g.141828_141830delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.521-53_521-51delinsATG
ENST00000700062.1:c.521-53_521-51delinsATG
ENST00000700065.1:n.2437-53_2437-51delinsATG
ENST00000700066.1:c.1941-53_1941-51delinsATG	ENSP00000514780.1:n.1941-53_1941-51delinsATG
ENST00000281513.10:c.2424-53_2424-51delinsATG MANE Select	ENSP00000281513.5:n.2424-53_2424-51delinsATG
ENST00000281513.9:c.2424-53_2424-51delinsATG	ENSP00000281513.5:n.2424-53_2424-51delinsATG
NM_015909.3:c.2424-53_2424-51delinsATG	NP_056993.2:n.2424-53_2424-51delinsATG
NR_052013.2:n.2468-53_2468-51delinsATG
XM_011510357.1:c.2295-53_2295-51delinsATG	XP_011508659.1:n.2295-53_2295-51delinsATG
XM_011510358.1:c.2424-53_2424-51delinsATG	XP_011508660.1:n.2424-53_2424-51delinsATG
XM_011510359.1:c.1785-53_1785-51delinsATG	XP_011508661.1:n.1785-53_1785-51delinsATG
XM_011510360.1:c.225-53_225-51delinsATG	XP_011508662.1:n.225-53_225-51delinsATG
XM_011510361.1:c.216-53_216-51delinsATG	XP_011508663.1:n.216-53_216-51delinsATG
XM_011510357.2:c.2295-53_2295-51delinsATG	XP_011508659.1:n.2295-53_2295-51delinsATG
XM_011510358.2:c.2424-53_2424-51delinsATG	XP_011508660.1:n.2424-53_2424-51delinsATG
XM_011510360.2:c.225-53_225-51delinsATG	XP_011508662.1:n.225-53_225-51delinsATG
XM_011510361.2:c.216-53_216-51delinsATG	XP_011508663.1:n.216-53_216-51delinsATG
XM_017004317.1:c.2424-53_2424-51delinsATG	XP_016859806.1:n.2424-53_2424-51delinsATG
XM_024452961.1:c.1785-53_1785-51delinsATG	XP_024308729.1:n.1785-53_1785-51delinsATG
NM_015909.4:c.2424-53_2424-51delinsATG MANE Select	NP_056993.2:n.2424-53_2424-51delinsATG
NR_052013.3:n.2454-53_2454-51delinsATG