Canonical Allele Identifier: CA1535060

Gene: NBAS

Linked Data

• ClinVar Variation Id: 2174257
• ClinVar RCV Id: RCV002585099
• dbSNP Id: rs200331420
• ExAC: 2:15359052 G / A
• gnomAD v2: 2-15359052-G-A
• gnomAD v3: 2-15218928-G-A
• gnomAD v4: 2-15218928-G-A
• MyVariant Identifiers: chr2:g.15359052G>A (hg19) ; chr2:g.15218928G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218928G>A , CM000664.2:g.15218928G>A	GRCh38
NC_000002.11:g.15359052G>A , CM000664.1:g.15359052G>A	GRCh37
NC_000002.10:g.15276503G>A	NCBI36
NG_032964.1:g.347421C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4263C>T
ENST00000700062.1:c.4426+13494C>T
ENST00000700063.1:c.788C>T
ENST00000700064.1:c.2133C>T
ENST00000281513.10:c.6277C>T MANE Select	ENSP00000281513.5:p.Arg2093Trp
ENST00000281513.9:c.6277C>T	ENSP00000281513.5:p.Arg2093Trp
ENST00000417461.5:c.512+13494C>T	ENSP00000392421.1:n.512+13494C>T
ENST00000442506.5:c.3420C>T
NM_015909.3:c.6277C>T	NP_056993.2:p.Arg2093Trp
NR_052013.2:n.6280+13494C>T
XM_011510357.1:c.6148C>T	XP_011508659.1:p.Arg2050Trp
XM_011510358.1:c.6277C>T	XP_011508660.1:p.Arg2093Trp
XM_011510359.1:c.5638C>T	XP_011508661.1:p.Arg1880Trp
XM_011510360.1:c.4078C>T	XP_011508662.1:p.Arg1360Trp
XM_011510361.1:c.4069C>T	XP_011508663.1:p.Arg1357Trp
XM_011510357.2:c.6148C>T	XP_011508659.1:p.Arg2050Trp
XM_011510358.2:c.6277C>T	XP_011508660.1:p.Arg2093Trp
XM_011510360.2:c.4078C>T	XP_011508662.1:p.Arg1360Trp
XM_011510361.2:c.4069C>T	XP_011508663.1:p.Arg1357Trp
XM_017004317.1:c.6277C>T	XP_016859806.1:p.Arg2093Trp
XM_024452961.1:c.5638C>T	XP_024308729.1:p.Arg1880Trp
NM_015909.4:c.6277C>T MANE Select	NP_056993.2:p.Arg2093Trp
NR_052013.3:n.6266+13494C>T