Canonical Allele Identifier: CA2490796236

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218897_15218898delinsAC , CM000664.2:g.15218897_15218898delinsAC	GRCh38
NC_000002.11:g.15359021_15359022delinsAC , CM000664.1:g.15359021_15359022delinsAC	GRCh37
NC_000002.10:g.15276472_15276473delinsAC	NCBI36
NG_032964.1:g.347451_347452delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.4293_4294delinsGT
ENST00000700062.1:c.4426+13524_4426+13525delinsGT
ENST00000700063.1:c.818_819delinsGT
ENST00000700064.1:c.2163_2164delinsGT
ENST00000281513.10:c.6307_6308delinsGT MANE Select	ENSP00000281513.5:p.Val2103=
ENST00000281513.9:c.6307_6308delinsGT	ENSP00000281513.5:p.Val2103=
ENST00000417461.5:c.512+13524_512+13525delinsGT	ENSP00000392421.1:n.512+13524_512+13525de...
ENST00000442506.5:c.3450_3451delinsGT
NM_015909.3:c.6307_6308delinsGT	NP_056993.2:p.Val2103=
NR_052013.2:n.6280+13524_6280+13525delinsGT
XM_011510357.1:c.6178_6179delinsGT	XP_011508659.1:p.Val2060=
XM_011510358.1:c.6307_6308delinsGT	XP_011508660.1:p.Val2103=
XM_011510359.1:c.5668_5669delinsGT	XP_011508661.1:p.Val1890=
XM_011510360.1:c.4108_4109delinsGT	XP_011508662.1:p.Val1370=
XM_011510361.1:c.4099_4100delinsGT	XP_011508663.1:p.Val1367=
XM_011510357.2:c.6178_6179delinsGT	XP_011508659.1:p.Val2060=
XM_011510358.2:c.6307_6308delinsGT	XP_011508660.1:p.Val2103=
XM_011510360.2:c.4108_4109delinsGT	XP_011508662.1:p.Val1370=
XM_011510361.2:c.4099_4100delinsGT	XP_011508663.1:p.Val1367=
XM_017004317.1:c.6307_6308delinsGT	XP_016859806.1:p.Val2103=
XM_024452961.1:c.5668_5669delinsGT	XP_024308729.1:p.Val1890=
NM_015909.4:c.6307_6308delinsGT MANE Select	NP_056993.2:p.Val2103=
NR_052013.3:n.6266+13524_6266+13525delinsGT