Canonical Allele Identifier: CA1206217003

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731965_169731968delinsTGAG , CM000663.2:g.169731965_169731968delinsTGAG	GRCh38
NC_000001.10:g.169701106_169701109delinsTGAG , CM000663.1:g.169701106_169701109delinsTGAG	GRCh37
NC_000001.9:g.167967730_167967733delinsTGAG	NCBI36
NG_012124.1:g.7112_7115delinsCTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.422-26_422-23delinsCTCA (SELE) MANE Select	ENSP00000331736.7:n.422-26_422-23delinsCTCA
ENST00000333360.11:c.422-26_422-23delinsCTCA (SELE)	ENSP00000331736.7:n.422-26_422-23delinsCTCA
ENST00000367774.1:c.422-26_422-23delinsCTCA (SELE)	ENSP00000356748.1:n.422-26_422-23delinsCTCA
ENST00000367775.5:c.422-26_422-23delinsCTCA (SELE)	ENSP00000356749.1:n.422-26_422-23delinsCTCA
ENST00000367776.5:c.422-26_422-23delinsCTCA (SELE)	ENSP00000356750.1:n.422-26_422-23delinsCTCA
ENST00000367777.5:c.422-26_422-23delinsCTCA (SELE)	ENSP00000356751.1:n.422-26_422-23delinsCTCA
ENST00000461085.1:n.105-26_105-23delinsCTCA (SELE)
ENST00000498289.5:n.851+48033_851+48036delinsTGAG (FIRRM)
NM_000450.2:c.422-26_422-23delinsCTCA (SELE) MANE Select	NP_000441.2:n.422-26_422-23delinsCTCA