Canonical Allele Identifier: CA759219629

Gene: NBAS

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15524632C>G , CM000664.2:g.15524632C>G	GRCh38
NC_000002.11:g.15664756C>G , CM000664.1:g.15664756C>G	GRCh37
NC_000002.10:g.15582207C>G	NCBI36
NG_032964.1:g.41717G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700065.1:n.759+9911G>C
ENST00000700066.1:c.263+9911G>C	ENSP00000514780.1:n.263+9911G>C
ENST00000700067.1:n.761+9911G>C
ENST00000700068.1:n.761+9911G>C
ENST00000700069.1:c.746+9911G>C	ENSP00000514781.1:n.746+9911G>C
ENST00000700070.1:c.*405+9911G>C	ENSP00000514782.1:n.*405+9911G>C
ENST00000700071.1:n.777-9401G>C
ENST00000281513.10:c.746+9911G>C MANE Select	ENSP00000281513.5:n.746+9911G>C
ENST00000281513.9:c.746+9911G>C	ENSP00000281513.5:n.746+9911G>C
NM_015909.3:c.746+9911G>C	NP_056993.2:n.746+9911G>C
NR_052013.2:n.790+9911G>C
XM_011510357.1:c.746+9911G>C	XP_011508659.1:n.746+9911G>C
XM_011510358.1:c.746+9911G>C	XP_011508660.1:n.746+9911G>C
XM_011510359.1:c.107+9911G>C	XP_011508661.1:n.107+9911G>C
XM_011510357.2:c.746+9911G>C	XP_011508659.1:n.746+9911G>C
XM_011510358.2:c.746+9911G>C	XP_011508660.1:n.746+9911G>C
XM_017004317.1:c.746+9911G>C	XP_016859806.1:n.746+9911G>C
XM_024452961.1:c.107+9911G>C	XP_024308729.1:n.107+9911G>C
NM_015909.4:c.746+9911G>C MANE Select	NP_056993.2:n.746+9911G>C
NR_052013.3:n.776+9911G>C