Canonical Allele Identifier: CA1787026121
Gene: NSMAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58595933T= , CM000670.2:g.58595933T= GRCh38
NC_000008.10:g.59508492T= , CM000670.1:g.59508492T= GRCh37
NC_000008.9:g.59671046T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000038176.8:c.1793-274A= MANE Select ENSP00000038176.3:n.1793-274A=
ENST00000649465.1:c.*1932-274A= ENSP00000498107.1:n.*1932-274A=
ENST00000038176.7:c.1793-274A= ENSP00000038176.3:n.1793-274A=
ENST00000427130.6:c.1886-274A= ENSP00000411012.2:n.1886-274A=
ENST00000523106.5:n.457-274A=
NM_001144772.1:c.1886-274A= NP_001138244.1:n.1886-274A=
NM_003580.3:c.1793-274A= NP_003571.2:n.1793-274A=
NM_003580.4:c.1793-274A= MANE Select NP_003571.2:n.1793-274A=