Canonical Allele Identifier: CA1535976

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15374701T>C , CM000664.2:g.15374701T>C	GRCh38
NC_000002.11:g.15514825T>C , CM000664.1:g.15514825T>C	GRCh37
NC_000002.10:g.15432276T>C	NCBI36
NG_032964.1:g.191648A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015909.4:c.3610A>G MANE Select	NP_056993.2:p.Thr1204Ala
ENST00000281513.10:c.3610A>G MANE Select	ENSP00000281513.5:p.Thr1204Ala
NM_015909.3:c.3610A>G	NP_056993.2:p.Thr1204Ala
NR_052013.2:n.3654A>G
NR_052013.3:n.3640A>G
ENST00000281513.9:c.3610A>G	ENSP00000281513.5:p.Thr1204Ala
ENST00000441755.5:c.751A>G	ENSP00000396501.1:p.Thr251Ala
ENST00000442506.5:c.753A>G
ENST00000700061.1:c.1707A>G
ENST00000700062.1:c.1707A>G
ENST00000700065.1:n.3623A>G
XM_011510357.1:c.3481A>G	XP_011508659.1:p.Thr1161Ala
XM_011510357.2:c.3481A>G	XP_011508659.1:p.Thr1161Ala
XM_011510358.1:c.3610A>G	XP_011508660.1:p.Thr1204Ala
XM_011510358.2:c.3610A>G	XP_011508660.1:p.Thr1204Ala
XM_011510359.1:c.2971A>G	XP_011508661.1:p.Thr991Ala
XM_011510360.1:c.1411A>G	XP_011508662.1:p.Thr471Ala
XM_011510360.2:c.1411A>G	XP_011508662.1:p.Thr471Ala
XM_011510361.1:c.1402A>G	XP_011508663.1:p.Thr468Ala
XM_011510361.2:c.1402A>G	XP_011508663.1:p.Thr468Ala
XM_017004317.1:c.3610A>G	XP_016859806.1:p.Thr1204Ala
XM_024452961.1:c.2971A>G	XP_024308729.1:p.Thr991Ala