Canonical Allele Identifier: CA1206216910

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731724_169731733delinsACACCATCTG , CM000663.2:g.169731724_169731733delinsACACCATCTG	GRCh38
NC_000001.10:g.169700865_169700874delinsACACCATCTG , CM000663.1:g.169700865_169700874delinsACACCATCTG	GRCh37
NC_000001.9:g.167967489_167967498delinsACACCATCTG	NCBI36
NG_012124.1:g.7347_7356delinsCAGATGGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.529+102_529+111delinsCAGATGGTGT (SELE) MANE Select	ENSP00000331736.7:n.529+102_529+111delinsCAGATGGTGT
ENST00000333360.11:c.529+102_529+111delinsCAGATGGTGT (SELE)	ENSP00000331736.7:n.529+102_529+111delinsCAGATGGTGT
ENST00000367774.1:c.529+102_529+111delinsCAGATGGTGT (SELE)	ENSP00000356748.1:n.529+102_529+111delinsCAGATGGTGT
ENST00000367775.5:c.529+102_529+111delinsCAGATGGTGT (SELE)	ENSP00000356749.1:n.529+102_529+111delinsCAGATGGTGT
ENST00000367776.5:c.529+102_529+111delinsCAGATGGTGT (SELE)	ENSP00000356750.1:n.529+102_529+111delinsCAGATGGTGT
ENST00000367777.5:c.529+102_529+111delinsCAGATGGTGT (SELE)	ENSP00000356751.1:n.529+102_529+111delinsCAGATGGTGT
ENST00000461085.1:n.314_323delinsCAGATGGTGT (SELE)
ENST00000498289.5:n.851+47792_851+47801delinsACACCATCTG (FIRRM)
NM_000450.2:c.529+102_529+111delinsCAGATGGTGT (SELE) MANE Select	NP_000441.2:n.529+102_529+111delinsCAGATGGTGT