Canonical Allele Identifier: CA1206216972

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731870C= , CM000663.2:g.169731870C=	GRCh38
NC_000001.10:g.169701011C= , CM000663.1:g.169701011C=	GRCh37
NC_000001.9:g.167967635C=	NCBI36
NG_012124.1:g.7210G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.494G= (SELE) MANE Select	ENSP00000331736.7:p.Cys165=
ENST00000333360.11:c.494G= (SELE)	ENSP00000331736.7:p.Cys165=
ENST00000367774.1:c.494G= (SELE)	ENSP00000356748.1:p.Cys165=
ENST00000367775.5:c.494G= (SELE)	ENSP00000356749.1:p.Cys165=
ENST00000367776.5:c.494G= (SELE)	ENSP00000356750.1:p.Cys165=
ENST00000367777.5:c.494G= (SELE)	ENSP00000356751.1:p.Cys165=
ENST00000461085.1:n.177G= (SELE)
ENST00000498289.5:n.851+47938C= (FIRRM)
NM_000450.2:c.494G= (SELE) MANE Select	NP_000441.2:p.Cys165=