Canonical Allele Identifier: CA345884724

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15359016G>A (hg19) ; chr2:g.15218892G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218892G>A , CM000664.2:g.15218892G>A	GRCh38
NC_000002.11:g.15359016G>A , CM000664.1:g.15359016G>A	GRCh37
NC_000002.10:g.15276467G>A	NCBI36
NG_032964.1:g.347457C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000700061.1:c.4299C>T
ENST00000700062.1:c.4426+13530C>T
ENST00000700063.1:c.824C>T
ENST00000700064.1:c.2169C>T
ENST00000281513.10:c.6313C>T MANE Select	ENSP00000281513.5:p.Pro2105Ser
ENST00000281513.9:c.6313C>T	ENSP00000281513.5:p.Pro2105Ser
ENST00000417461.5:c.512+13530C>T	ENSP00000392421.1:n.512+13530C>T
ENST00000442506.5:c.3456C>T
NM_015909.3:c.6313C>T	NP_056993.2:p.Pro2105Ser
NR_052013.2:n.6280+13530C>T
XM_011510357.1:c.6184C>T	XP_011508659.1:p.Pro2062Ser
XM_011510358.1:c.6313C>T	XP_011508660.1:p.Pro2105Ser
XM_011510359.1:c.5674C>T	XP_011508661.1:p.Pro1892Ser
XM_011510360.1:c.4114C>T	XP_011508662.1:p.Pro1372Ser
XM_011510361.1:c.4105C>T	XP_011508663.1:p.Pro1369Ser
XM_011510357.2:c.6184C>T	XP_011508659.1:p.Pro2062Ser
XM_011510358.2:c.6313C>T	XP_011508660.1:p.Pro2105Ser
XM_011510360.2:c.4114C>T	XP_011508662.1:p.Pro1372Ser
XM_011510361.2:c.4105C>T	XP_011508663.1:p.Pro1369Ser
XM_017004317.1:c.6313C>T	XP_016859806.1:p.Pro2105Ser
XM_024452961.1:c.5674C>T	XP_024308729.1:p.Pro1892Ser
NM_015909.4:c.6313C>T MANE Select	NP_056993.2:p.Pro2105Ser
NR_052013.3:n.6266+13530C>T