Canonical Allele Identifier: CA345881974

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15542336A>C (hg19) ; chr2:g.15402212A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402212A>C , CM000664.2:g.15402212A>C	GRCh38
NC_000002.11:g.15542336A>C , CM000664.1:g.15542336A>C	GRCh37
NC_000002.10:g.15459787A>C	NCBI36
NG_032964.1:g.164137T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1124T>G
ENST00000700062.1:c.1124T>G
ENST00000700065.1:n.3040T>G
ENST00000281513.10:c.3027T>G MANE Select	ENSP00000281513.5:p.Cys1009Trp
ENST00000281513.9:c.3027T>G	ENSP00000281513.5:p.Cys1009Trp
ENST00000429842.1:c.319T>G
ENST00000441755.5:c.168T>G	ENSP00000396501.1:p.Cys56Trp
ENST00000442506.5:c.170T>G
NM_015909.3:c.3027T>G	NP_056993.2:p.Cys1009Trp
NR_052013.2:n.3071T>G
XM_011510357.1:c.2898T>G	XP_011508659.1:p.Cys966Trp
XM_011510358.1:c.3027T>G	XP_011508660.1:p.Cys1009Trp
XM_011510359.1:c.2388T>G	XP_011508661.1:p.Cys796Trp
XM_011510360.1:c.828T>G	XP_011508662.1:p.Cys276Trp
XM_011510361.1:c.819T>G	XP_011508663.1:p.Cys273Trp
XM_011510357.2:c.2898T>G	XP_011508659.1:p.Cys966Trp
XM_011510358.2:c.3027T>G	XP_011508660.1:p.Cys1009Trp
XM_011510360.2:c.828T>G	XP_011508662.1:p.Cys276Trp
XM_011510361.2:c.819T>G	XP_011508663.1:p.Cys273Trp
XM_017004317.1:c.3027T>G	XP_016859806.1:p.Cys1009Trp
XM_024452961.1:c.2388T>G	XP_024308729.1:p.Cys796Trp
NM_015909.4:c.3027T>G MANE Select	NP_056993.2:p.Cys1009Trp
NR_052013.3:n.3057T>G