Canonical Allele Identifier: CA1536391

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15461163_15461164insT , CM000664.2:g.15461163_15461164insT	GRCh38
NC_000002.11:g.15601287_15601288insT , CM000664.1:g.15601287_15601288insT	GRCh37
NC_000002.10:g.15518738_15518739insT	NCBI36
NG_032964.1:g.105185_105186insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.436+37_436+38insA
ENST00000700062.1:c.436+37_436+38insA
ENST00000700065.1:n.2352+37_2352+38insA
ENST00000700066.1:c.1856+37_1856+38insA	ENSP00000514780.1:n.1856+37_1856+38insA
ENST00000700067.1:n.2354+37_2354+38insA
ENST00000700068.1:n.2391_2392insA
ENST00000281513.10:c.2339+37_2339+38insA MANE Select	ENSP00000281513.5:n.2339+37_2339+38insA
ENST00000281513.9:c.2339+37_2339+38insA	ENSP00000281513.5:n.2339+37_2339+38insA
NM_015909.3:c.2339+37_2339+38insA	NP_056993.2:n.2339+37_2339+38insA
NR_052013.2:n.2383+37_2383+38insA
XM_011510357.1:c.2210+37_2210+38insA	XP_011508659.1:n.2210+37_2210+38insA
XM_011510358.1:c.2339+37_2339+38insA	XP_011508660.1:n.2339+37_2339+38insA
XM_011510359.1:c.1700+37_1700+38insA	XP_011508661.1:n.1700+37_1700+38insA
XM_011510357.2:c.2210+37_2210+38insA	XP_011508659.1:n.2210+37_2210+38insA
XM_011510358.2:c.2339+37_2339+38insA	XP_011508660.1:n.2339+37_2339+38insA
XM_017004317.1:c.2339+37_2339+38insA	XP_016859806.1:n.2339+37_2339+38insA
XM_024452961.1:c.1700+37_1700+38insA	XP_024308729.1:n.1700+37_1700+38insA
NM_015909.4:c.2339+37_2339+38insA MANE Select	NP_056993.2:n.2339+37_2339+38insA
NR_052013.3:n.2369+37_2369+38insA