Canonical Allele Identifier: CA345884138

Gene: NBAS

Linked Data

• MyVariant Identifiers: chr2:g.15358962C>A (hg19) ; chr2:g.15218838C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15218838C>A , CM000664.2:g.15218838C>A	GRCh38
NC_000002.11:g.15358962C>A , CM000664.1:g.15358962C>A	GRCh37
NC_000002.10:g.15276413C>A	NCBI36
NG_032964.1:g.347511G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700061.1:c.4353G>T
ENST00000700062.1:c.4426+13584G>T
ENST00000700063.1:c.878G>T
ENST00000700064.1:c.2223G>T
ENST00000281513.10:c.6367G>T MANE Select	ENSP00000281513.5:p.Asp2123Tyr
ENST00000281513.9:c.6367G>T	ENSP00000281513.5:p.Asp2123Tyr
ENST00000417461.5:c.512+13584G>T	ENSP00000392421.1:n.512+13584G>T
ENST00000442506.5:c.3510G>T
NM_015909.3:c.6367G>T	NP_056993.2:p.Asp2123Tyr
NR_052013.2:n.6280+13584G>T
XM_011510357.1:c.6238G>T	XP_011508659.1:p.Asp2080Tyr
XM_011510358.1:c.6367G>T	XP_011508660.1:p.Asp2123Tyr
XM_011510359.1:c.5728G>T	XP_011508661.1:p.Asp1910Tyr
XM_011510360.1:c.4168G>T	XP_011508662.1:p.Asp1390Tyr
XM_011510361.1:c.4159G>T	XP_011508663.1:p.Asp1387Tyr
XM_011510357.2:c.6238G>T	XP_011508659.1:p.Asp2080Tyr
XM_011510358.2:c.6367G>T	XP_011508660.1:p.Asp2123Tyr
XM_011510360.2:c.4168G>T	XP_011508662.1:p.Asp1390Tyr
XM_011510361.2:c.4159G>T	XP_011508663.1:p.Asp1387Tyr
XM_017004317.1:c.6367G>T	XP_016859806.1:p.Asp2123Tyr
XM_024452961.1:c.5728G>T	XP_024308729.1:p.Asp1910Tyr
NM_015909.4:c.6367G>T MANE Select	NP_056993.2:p.Asp2123Tyr
NR_052013.3:n.6266+13584G>T