Canonical Allele Identifier: CA1535373

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15287049C>T , CM000664.2:g.15287049C>T	GRCh38
NC_000002.11:g.15427173C>T , CM000664.1:g.15427173C>T	GRCh37
NC_000002.10:g.15344624C>T	NCBI36
NG_032964.1:g.279300G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015909.4:c.5138+24G>A MANE Select	NP_056993.2:n.5138+24G>A
ENST00000281513.10:c.5138+24G>A MANE Select	ENSP00000281513.5:n.5138+24G>A
NM_015909.3:c.5138+24G>A	NP_056993.2:n.5138+24G>A
NR_052013.2:n.5182+24G>A
NR_052013.3:n.5168+24G>A
ENST00000281513.9:c.5138+24G>A	ENSP00000281513.5:n.5138+24G>A
ENST00000442506.5:c.2281+24G>A
ENST00000700061.1:c.3124+5488G>A
ENST00000700062.1:c.3328+24G>A
ENST00000700064.1:c.994+24G>A
XM_011510357.1:c.5009+24G>A	XP_011508659.1:n.5009+24G>A
XM_011510357.2:c.5009+24G>A	XP_011508659.1:n.5009+24G>A
XM_011510358.1:c.5138+24G>A	XP_011508660.1:n.5138+24G>A
XM_011510358.2:c.5138+24G>A	XP_011508660.1:n.5138+24G>A
XM_011510359.1:c.4499+24G>A	XP_011508661.1:n.4499+24G>A
XM_011510360.1:c.2939+24G>A	XP_011508662.1:n.2939+24G>A
XM_011510360.2:c.2939+24G>A	XP_011508662.1:n.2939+24G>A
XM_011510361.1:c.2930+24G>A	XP_011508663.1:n.2930+24G>A
XM_011510361.2:c.2930+24G>A	XP_011508663.1:n.2930+24G>A
XM_017004317.1:c.5138+24G>A	XP_016859806.1:n.5138+24G>A
XM_024452961.1:c.4499+24G>A	XP_024308729.1:n.4499+24G>A