Canonical Allele Identifier: CA1787026133
Gene: NSMAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58595959C= , CM000670.2:g.58595959C= GRCh38
NC_000008.10:g.59508518C= , CM000670.1:g.59508518C= GRCh37
NC_000008.9:g.59671072C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000038176.8:c.1793-300G= MANE Select ENSP00000038176.3:n.1793-300G=
ENST00000649465.1:c.*1932-300G= ENSP00000498107.1:n.*1932-300G=
ENST00000038176.7:c.1793-300G= ENSP00000038176.3:n.1793-300G=
ENST00000427130.6:c.1886-300G= ENSP00000411012.2:n.1886-300G=
ENST00000523106.5:n.457-300G=
NM_001144772.1:c.1886-300G= NP_001138244.1:n.1886-300G=
NM_003580.3:c.1793-300G= NP_003571.2:n.1793-300G=
NM_003580.4:c.1793-300G= MANE Select NP_003571.2:n.1793-300G=