Canonical Allele Identifier: CA1206216960

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731841C= , CM000663.2:g.169731841C=	GRCh38
NC_000001.10:g.169700982C= , CM000663.1:g.169700982C=	GRCh37
NC_000001.9:g.167967606C=	NCBI36
NG_012124.1:g.7239G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.523G= (SELE) MANE Select	ENSP00000331736.7:p.Glu175=
ENST00000333360.11:c.523G= (SELE)	ENSP00000331736.7:p.Glu175=
ENST00000367774.1:c.523G= (SELE)	ENSP00000356748.1:p.Glu175=
ENST00000367775.5:c.523G= (SELE)	ENSP00000356749.1:p.Glu175=
ENST00000367776.5:c.523G= (SELE)	ENSP00000356750.1:p.Glu175=
ENST00000367777.5:c.523G= (SELE)	ENSP00000356751.1:p.Glu175=
ENST00000461085.1:n.206G= (SELE)
ENST00000498289.5:n.851+47909C= (FIRRM)
NM_000450.2:c.523G= (SELE) MANE Select	NP_000441.2:p.Glu175=