Canonical Allele Identifier: CA1787026132

Gene: NSMAF

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58595952G= , CM000670.2:g.58595952G=	GRCh38
NC_000008.10:g.59508511G= , CM000670.1:g.59508511G=	GRCh37
NC_000008.9:g.59671065G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000038176.8:c.1793-293C= MANE Select	ENSP00000038176.3:n.1793-293C=
ENST00000649465.1:c.*1932-293C=	ENSP00000498107.1:n.*1932-293C=
ENST00000038176.7:c.1793-293C=	ENSP00000038176.3:n.1793-293C=
ENST00000427130.6:c.1886-293C=	ENSP00000411012.2:n.1886-293C=
ENST00000523106.5:n.457-293C=
NM_001144772.1:c.1886-293C=	NP_001138244.1:n.1886-293C=
NM_003580.3:c.1793-293C=	NP_003571.2:n.1793-293C=
NM_003580.4:c.1793-293C= MANE Select	NP_003571.2:n.1793-293C=