Canonical Allele Identifier: CA345882497

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15542422G>T (hg19) ; chr2:g.15402298G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402298G>T , CM000664.2:g.15402298G>T	GRCh38
NC_000002.11:g.15542422G>T , CM000664.1:g.15542422G>T	GRCh37
NC_000002.10:g.15459873G>T	NCBI36
NG_032964.1:g.164051C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.1038C>A
ENST00000700062.1:c.1038C>A
ENST00000700065.1:n.2954C>A
ENST00000281513.10:c.2941C>A MANE Select	ENSP00000281513.5:p.Gln981Lys
ENST00000281513.9:c.2941C>A	ENSP00000281513.5:p.Gln981Lys
ENST00000429842.1:c.233C>A
ENST00000441755.5:c.82C>A	ENSP00000396501.1:p.Gln28Lys
ENST00000442506.5:c.84C>A
NM_015909.3:c.2941C>A	NP_056993.2:p.Gln981Lys
NR_052013.2:n.2985C>A
XM_011510357.1:c.2812C>A	XP_011508659.1:p.Gln938Lys
XM_011510358.1:c.2941C>A	XP_011508660.1:p.Gln981Lys
XM_011510359.1:c.2302C>A	XP_011508661.1:p.Gln768Lys
XM_011510360.1:c.742C>A	XP_011508662.1:p.Gln248Lys
XM_011510361.1:c.733C>A	XP_011508663.1:p.Gln245Lys
XM_011510357.2:c.2812C>A	XP_011508659.1:p.Gln938Lys
XM_011510358.2:c.2941C>A	XP_011508660.1:p.Gln981Lys
XM_011510360.2:c.742C>A	XP_011508662.1:p.Gln248Lys
XM_011510361.2:c.733C>A	XP_011508663.1:p.Gln245Lys
XM_017004317.1:c.2941C>A	XP_016859806.1:p.Gln981Lys
XM_024452961.1:c.2302C>A	XP_024308729.1:p.Gln768Lys
NM_015909.4:c.2941C>A MANE Select	NP_056993.2:p.Gln981Lys
NR_052013.3:n.2971C>A