Canonical Allele Identifier: CA1787026123
Gene: NSMAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58595936G= , CM000670.2:g.58595936G= GRCh38
NC_000008.10:g.59508495G= , CM000670.1:g.59508495G= GRCh37
NC_000008.9:g.59671049G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000038176.8:c.1793-277C= MANE Select ENSP00000038176.3:n.1793-277C=
ENST00000649465.1:c.*1932-277C= ENSP00000498107.1:n.*1932-277C=
ENST00000038176.7:c.1793-277C= ENSP00000038176.3:n.1793-277C=
ENST00000427130.6:c.1886-277C= ENSP00000411012.2:n.1886-277C=
ENST00000523106.5:n.457-277C=
NM_001144772.1:c.1886-277C= NP_001138244.1:n.1886-277C=
NM_003580.3:c.1793-277C= NP_003571.2:n.1793-277C=
NM_003580.4:c.1793-277C= MANE Select NP_003571.2:n.1793-277C=