Canonical Allele Identifier: CA345890155

Gene: NBAS

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15292721G>A , CM000664.2:g.15292721G>A	GRCh38
NC_000002.11:g.15432845G>A , CM000664.1:g.15432845G>A	GRCh37
NC_000002.10:g.15350296G>A	NCBI36
NG_032964.1:g.273628C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015909.4:c.4843C>T MANE Select	NP_056993.2:p.Arg1615Ter
ENST00000281513.10:c.4843C>T MANE Select	ENSP00000281513.5:p.Arg1615Ter
NM_015909.3:c.4843C>T	NP_056993.2:p.Arg1615Ter
NR_052013.2:n.4887C>T
NR_052013.3:n.4873C>T
ENST00000281513.9:c.4843C>T	ENSP00000281513.5:p.Arg1615Ter
ENST00000442506.5:c.1986C>T
ENST00000700061.1:c.2940C>T
ENST00000700062.1:c.3033C>T
ENST00000700064.1:c.699C>T
XM_011510357.1:c.4714C>T	XP_011508659.1:p.Arg1572Ter
XM_011510357.2:c.4714C>T	XP_011508659.1:p.Arg1572Ter
XM_011510358.1:c.4843C>T	XP_011508660.1:p.Arg1615Ter
XM_011510358.2:c.4843C>T	XP_011508660.1:p.Arg1615Ter
XM_011510359.1:c.4204C>T	XP_011508661.1:p.Arg1402Ter
XM_011510360.1:c.2644C>T	XP_011508662.1:p.Arg882Ter
XM_011510360.2:c.2644C>T	XP_011508662.1:p.Arg882Ter
XM_011510361.1:c.2635C>T	XP_011508663.1:p.Arg879Ter
XM_011510361.2:c.2635C>T	XP_011508663.1:p.Arg879Ter
XM_017004317.1:c.4843C>T	XP_016859806.1:p.Arg1615Ter
XM_024452961.1:c.4204C>T	XP_024308729.1:p.Arg1402Ter