Canonical Allele Identifier: CA2687375236
Gene: NSMAF HGNC NCBI

Linked Data

gnomAD v4: 8-58595943-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.58595943T>C , CM000670.2:g.58595943T>C GRCh38
NC_000008.10:g.59508502T>C , CM000670.1:g.59508502T>C GRCh37
NC_000008.9:g.59671056T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000038176.8:c.1793-284A>G MANE Select ENSP00000038176.3:n.1793-284A>G
ENST00000649465.1:c.*1932-284A>G ENSP00000498107.1:n.*1932-284A>G
ENST00000038176.7:c.1793-284A>G ENSP00000038176.3:n.1793-284A>G
ENST00000427130.6:c.1886-284A>G ENSP00000411012.2:n.1886-284A>G
ENST00000523106.5:n.457-284A>G
NM_001144772.1:c.1886-284A>G NP_001138244.1:n.1886-284A>G
NM_003580.3:c.1793-284A>G NP_003571.2:n.1793-284A>G
NM_003580.4:c.1793-284A>G MANE Select NP_003571.2:n.1793-284A>G