Canonical Allele Identifier: CA345884545

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15358992A>T (hg19) ; chr2:g.15218868A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218868A>T , CM000664.2:g.15218868A>T	GRCh38
NC_000002.11:g.15358992A>T , CM000664.1:g.15358992A>T	GRCh37
NC_000002.10:g.15276443A>T	NCBI36
NG_032964.1:g.347481T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4323T>A
ENST00000700062.1:c.4426+13554T>A
ENST00000700063.1:c.848T>A
ENST00000700064.1:c.2193T>A
ENST00000281513.10:c.6337T>A MANE Select	ENSP00000281513.5:p.Leu2113Met
ENST00000281513.9:c.6337T>A	ENSP00000281513.5:p.Leu2113Met
ENST00000417461.5:c.512+13554T>A	ENSP00000392421.1:n.512+13554T>A
ENST00000442506.5:c.3480T>A
NM_015909.3:c.6337T>A	NP_056993.2:p.Leu2113Met
NR_052013.2:n.6280+13554T>A
XM_011510357.1:c.6208T>A	XP_011508659.1:p.Leu2070Met
XM_011510358.1:c.6337T>A	XP_011508660.1:p.Leu2113Met
XM_011510359.1:c.5698T>A	XP_011508661.1:p.Leu1900Met
XM_011510360.1:c.4138T>A	XP_011508662.1:p.Leu1380Met
XM_011510361.1:c.4129T>A	XP_011508663.1:p.Leu1377Met
XM_011510357.2:c.6208T>A	XP_011508659.1:p.Leu2070Met
XM_011510358.2:c.6337T>A	XP_011508660.1:p.Leu2113Met
XM_011510360.2:c.4138T>A	XP_011508662.1:p.Leu1380Met
XM_011510361.2:c.4129T>A	XP_011508663.1:p.Leu1377Met
XM_017004317.1:c.6337T>A	XP_016859806.1:p.Leu2113Met
XM_024452961.1:c.5698T>A	XP_024308729.1:p.Leu1900Met
NM_015909.4:c.6337T>A MANE Select	NP_056993.2:p.Leu2113Met
NR_052013.3:n.6266+13554T>A