Canonical Allele Identifier: CA1787026128
Gene: NSMAF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58595947A= , CM000670.2:g.58595947A= GRCh38
NC_000008.10:g.59508506A= , CM000670.1:g.59508506A= GRCh37
NC_000008.9:g.59671060A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000038176.8:c.1793-288T= MANE Select ENSP00000038176.3:n.1793-288T=
ENST00000649465.1:c.*1932-288T= ENSP00000498107.1:n.*1932-288T=
ENST00000038176.7:c.1793-288T= ENSP00000038176.3:n.1793-288T=
ENST00000427130.6:c.1886-288T= ENSP00000411012.2:n.1886-288T=
ENST00000523106.5:n.457-288T=
NM_001144772.1:c.1886-288T= NP_001138244.1:n.1886-288T=
NM_003580.3:c.1793-288T= NP_003571.2:n.1793-288T=
NM_003580.4:c.1793-288T= MANE Select NP_003571.2:n.1793-288T=
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