Canonical Allele Identifier: CA345881880

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15542307G>T (hg19) ; chr2:g.15402183G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15402183G>T , CM000664.2:g.15402183G>T	GRCh38
NC_000002.11:g.15542307G>T , CM000664.1:g.15542307G>T	GRCh37
NC_000002.10:g.15459758G>T	NCBI36
NG_032964.1:g.164166C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.1153C>A
ENST00000700062.1:c.1153C>A
ENST00000700065.1:n.3069C>A
ENST00000281513.10:c.3056C>A MANE Select	ENSP00000281513.5:p.Pro1019Gln
ENST00000281513.9:c.3056C>A	ENSP00000281513.5:p.Pro1019Gln
ENST00000429842.1:c.348C>A
ENST00000441755.5:c.197C>A	ENSP00000396501.1:p.Pro66Gln
ENST00000442506.5:c.199C>A
NM_015909.3:c.3056C>A	NP_056993.2:p.Pro1019Gln
NR_052013.2:n.3100C>A
XM_011510357.1:c.2927C>A	XP_011508659.1:p.Pro976Gln
XM_011510358.1:c.3056C>A	XP_011508660.1:p.Pro1019Gln
XM_011510359.1:c.2417C>A	XP_011508661.1:p.Pro806Gln
XM_011510360.1:c.857C>A	XP_011508662.1:p.Pro286Gln
XM_011510361.1:c.848C>A	XP_011508663.1:p.Pro283Gln
XM_011510357.2:c.2927C>A	XP_011508659.1:p.Pro976Gln
XM_011510358.2:c.3056C>A	XP_011508660.1:p.Pro1019Gln
XM_011510360.2:c.857C>A	XP_011508662.1:p.Pro286Gln
XM_011510361.2:c.848C>A	XP_011508663.1:p.Pro283Gln
XM_017004317.1:c.3056C>A	XP_016859806.1:p.Pro1019Gln
XM_024452961.1:c.2417C>A	XP_024308729.1:p.Pro806Gln
NM_015909.4:c.3056C>A MANE Select	NP_056993.2:p.Pro1019Gln
NR_052013.3:n.3086C>A