Canonical Allele Identifier: CA2532039680
Gene: NSMAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58595964C>A , CM000670.2:g.58595964C>A GRCh38
NC_000008.10:g.59508523C>A , CM000670.1:g.59508523C>A GRCh37
NC_000008.9:g.59671077C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000038176.8:c.1793-305G>T MANE Select ENSP00000038176.3:n.1793-305G>T
ENST00000649465.1:c.*1932-305G>T ENSP00000498107.1:n.*1932-305G>T
ENST00000038176.7:c.1793-305G>T ENSP00000038176.3:n.1793-305G>T
ENST00000427130.6:c.1886-305G>T ENSP00000411012.2:n.1886-305G>T
ENST00000523106.5:n.457-305G>T
NM_001144772.1:c.1886-305G>T NP_001138244.1:n.1886-305G>T
NM_003580.3:c.1793-305G>T NP_003571.2:n.1793-305G>T
NM_003580.4:c.1793-305G>T MANE Select NP_003571.2:n.1793-305G>T