Canonical Allele Identifier: CA1027860738

Gene: NBAS

Linked Data

• dbSNP Id: rs1676197701

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402344_15402354del , CM000664.2:g.15402344_15402354del	GRCh38
NC_000002.11:g.15542468_15542478del , CM000664.1:g.15542468_15542478del	GRCh37
NC_000002.10:g.15459919_15459929del	NCBI36
NG_032964.1:g.163999_164009del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.1035-49_1035-39del
ENST00000700062.1:c.1035-49_1035-39del
ENST00000700065.1:n.2951-49_2951-39del
ENST00000281513.10:c.2938-49_2938-39del MANE Select	ENSP00000281513.5:n.2938-49_2938-39del
ENST00000281513.9:c.2938-49_2938-39del	ENSP00000281513.5:n.2938-49_2938-39del
ENST00000429842.1:c.230-49_230-39del
ENST00000441755.5:c.79-49_79-39del	ENSP00000396501.1:n.79-49_79-39del
ENST00000442506.5:c.81-49_81-39del
NM_015909.3:c.2938-49_2938-39del	NP_056993.2:n.2938-49_2938-39del
NR_052013.2:n.2982-49_2982-39del
XM_011510357.1:c.2809-49_2809-39del	XP_011508659.1:n.2809-49_2809-39del
XM_011510358.1:c.2938-49_2938-39del	XP_011508660.1:n.2938-49_2938-39del
XM_011510359.1:c.2299-49_2299-39del	XP_011508661.1:n.2299-49_2299-39del
XM_011510360.1:c.739-49_739-39del	XP_011508662.1:n.739-49_739-39del
XM_011510361.1:c.730-49_730-39del	XP_011508663.1:n.730-49_730-39del
XM_011510357.2:c.2809-49_2809-39del	XP_011508659.1:n.2809-49_2809-39del
XM_011510358.2:c.2938-49_2938-39del	XP_011508660.1:n.2938-49_2938-39del
XM_011510360.2:c.739-49_739-39del	XP_011508662.1:n.739-49_739-39del
XM_011510361.2:c.730-49_730-39del	XP_011508663.1:n.730-49_730-39del
XM_017004317.1:c.2938-49_2938-39del	XP_016859806.1:n.2938-49_2938-39del
XM_024452961.1:c.2299-49_2299-39del	XP_024308729.1:n.2299-49_2299-39del
NM_015909.4:c.2938-49_2938-39del MANE Select	NP_056993.2:n.2938-49_2938-39del
NR_052013.3:n.2968-49_2968-39del