Canonical Allele Identifier: CA2780482299

Gene: NSMAF

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.58595933_58595941del , CM000670.2:g.58595933_58595941del	GRCh38
NC_000008.10:g.59508492_59508500del , CM000670.1:g.59508492_59508500del	GRCh37
NC_000008.9:g.59671046_59671054del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000038176.8:c.1793-279_1793-271del MANE Select	ENSP00000038176.3:n.1793-279_1793-271del
ENST00000649465.1:c.*1932-279_*1932-271del	ENSP00000498107.1:n.*1932-279_*1932-271del
ENST00000038176.7:c.1793-279_1793-271del	ENSP00000038176.3:n.1793-279_1793-271del
ENST00000427130.6:c.1886-279_1886-271del	ENSP00000411012.2:n.1886-279_1886-271del
ENST00000523106.5:n.457-279_457-271del
NM_001144772.1:c.1886-279_1886-271del	NP_001138244.1:n.1886-279_1886-271del
NM_003580.3:c.1793-279_1793-271del	NP_003571.2:n.1793-279_1793-271del
NM_003580.4:c.1793-279_1793-271del MANE Select	NP_003571.2:n.1793-279_1793-271del