Canonical Allele Identifier: CA11058465

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15374348A>C , CM000664.2:g.15374348A>C	GRCh38
NC_000002.11:g.15514472A>C , CM000664.1:g.15514472A>C	GRCh37
NC_000002.10:g.15431923A>C	NCBI36
NG_032964.1:g.192001T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_015909.4:c.3703+260T>G MANE Select	NP_056993.2:n.3703+260T>G
ENST00000281513.10:c.3703+260T>G MANE Select	ENSP00000281513.5:n.3703+260T>G
NM_015909.3:c.3703+260T>G	NP_056993.2:n.3703+260T>G
NR_052013.2:n.3747+260T>G
NR_052013.3:n.3733+260T>G
ENST00000281513.9:c.3703+260T>G	ENSP00000281513.5:n.3703+260T>G
ENST00000442506.5:c.846+260T>G
ENST00000700061.1:c.1800+260T>G
ENST00000700062.1:c.1800+260T>G
ENST00000700065.1:n.3716+260T>G
XM_011510357.1:c.3574+260T>G	XP_011508659.1:n.3574+260T>G
XM_011510357.2:c.3574+260T>G	XP_011508659.1:n.3574+260T>G
XM_011510358.1:c.3703+260T>G	XP_011508660.1:n.3703+260T>G
XM_011510358.2:c.3703+260T>G	XP_011508660.1:n.3703+260T>G
XM_011510359.1:c.3064+260T>G	XP_011508661.1:n.3064+260T>G
XM_011510360.1:c.1504+260T>G	XP_011508662.1:n.1504+260T>G
XM_011510360.2:c.1504+260T>G	XP_011508662.1:n.1504+260T>G
XM_011510361.1:c.1495+260T>G	XP_011508663.1:n.1495+260T>G
XM_011510361.2:c.1495+260T>G	XP_011508663.1:n.1495+260T>G
XM_017004317.1:c.3703+260T>G	XP_016859806.1:n.3703+260T>G
XM_024452961.1:c.3064+260T>G	XP_024308729.1:n.3064+260T>G