Canonical Allele Identifier: CA1140597851

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731503_169731505delinsGGG , CM000663.2:g.169731503_169731505delinsGGG	GRCh38
NC_000001.10:g.169700644_169700646delinsGGG , CM000663.1:g.169700644_169700646delinsGGG	GRCh37
NC_000001.9:g.167967268_167967270delinsGGG	NCBI36
NG_012124.1:g.7575_7577delinsCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.529+330_529+332delinsCCC (SELE) MANE Select	ENSP00000331736.7:n.529+330_529+332delinsCCC
ENST00000333360.11:c.529+330_529+332delinsCCC (SELE)	ENSP00000331736.7:n.529+330_529+332delinsCCC
ENST00000367774.1:c.529+330_529+332delinsCCC (SELE)	ENSP00000356748.1:n.529+330_529+332delinsCCC
ENST00000367775.5:c.529+330_529+332delinsCCC (SELE)	ENSP00000356749.1:n.529+330_529+332delinsCCC
ENST00000367776.5:c.529+330_529+332delinsCCC (SELE)	ENSP00000356750.1:n.529+330_529+332delinsCCC
ENST00000367777.5:c.529+330_529+332delinsCCC (SELE)	ENSP00000356751.1:n.529+330_529+332delinsCCC
ENST00000461085.1:n.542_544delinsCCC (SELE)
ENST00000498289.5:n.851+47571_851+47573delinsGGG (FIRRM)
NM_000450.2:c.529+330_529+332delinsCCC (SELE) MANE Select	NP_000441.2:n.529+330_529+332delinsCCC