Canonical Allele Identifier: CA853675112

Gene: NSMAF

Linked Data

• dbSNP Id: rs1421649141
• MyVariant Identifiers: chr8:g.59508495G>A (hg19) ; chr8:g.58595936G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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