Canonical Allele Identifier: CA345884624

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15359001G>T (hg19) ; chr2:g.15218877G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218877G>T , CM000664.2:g.15218877G>T	GRCh38
NC_000002.11:g.15359001G>T , CM000664.1:g.15359001G>T	GRCh37
NC_000002.10:g.15276452G>T	NCBI36
NG_032964.1:g.347472C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4314C>A
ENST00000700062.1:c.4426+13545C>A
ENST00000700063.1:c.839C>A
ENST00000700064.1:c.2184C>A
ENST00000281513.10:c.6328C>A MANE Select	ENSP00000281513.5:p.Leu2110Met
ENST00000281513.9:c.6328C>A	ENSP00000281513.5:p.Leu2110Met
ENST00000417461.5:c.512+13545C>A	ENSP00000392421.1:n.512+13545C>A
ENST00000442506.5:c.3471C>A
NM_015909.3:c.6328C>A	NP_056993.2:p.Leu2110Met
NR_052013.2:n.6280+13545C>A
XM_011510357.1:c.6199C>A	XP_011508659.1:p.Leu2067Met
XM_011510358.1:c.6328C>A	XP_011508660.1:p.Leu2110Met
XM_011510359.1:c.5689C>A	XP_011508661.1:p.Leu1897Met
XM_011510360.1:c.4129C>A	XP_011508662.1:p.Leu1377Met
XM_011510361.1:c.4120C>A	XP_011508663.1:p.Leu1374Met
XM_011510357.2:c.6199C>A	XP_011508659.1:p.Leu2067Met
XM_011510358.2:c.6328C>A	XP_011508660.1:p.Leu2110Met
XM_011510360.2:c.4129C>A	XP_011508662.1:p.Leu1377Met
XM_011510361.2:c.4120C>A	XP_011508663.1:p.Leu1374Met
XM_017004317.1:c.6328C>A	XP_016859806.1:p.Leu2110Met
XM_024452961.1:c.5689C>A	XP_024308729.1:p.Leu1897Met
NM_015909.4:c.6328C>A MANE Select	NP_056993.2:p.Leu2110Met
NR_052013.3:n.6266+13545C>A