Canonical Allele Identifier: CA409655638

Gene: STMN3

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63643872T>C , CM000682.2:g.63643872T>C	GRCh38
NC_000020.10:g.62275225T>C , CM000682.1:g.62275225T>C	GRCh37
NC_000020.9:g.61745669T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_015894.4:c.175A>G MANE Select	NP_056978.2:p.Lys59Glu
ENST00000370053.3:c.175A>G MANE Select	ENSP00000359070.1:p.Lys59Glu
NM_001276310.1:c.142A>G	NP_001263239.1:p.Lys48Glu
NM_001276310.2:c.142A>G	NP_001263239.1:p.Lys48Glu
NM_015894.3:c.175A>G	NP_056978.2:p.Lys59Glu
NR_075070.1:n.440A>G
NR_075070.2:n.254A>G
ENST00000370053.2:c.175A>G	ENSP00000359070.1:p.Lys59Glu
ENST00000540534.5:c.142A>G	ENSP00000439840.1:p.Lys48Glu
ENST00000631920.1:c.350A>G
ENST00000632676.1:c.142A>G	ENSP00000487639.1:p.Lys48Glu
ENST00000634126.1:c.142A>G	ENSP00000488604.1:p.Lys48Glu