Canonical Allele Identifier: CA1206216992

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731931T= , CM000663.2:g.169731931T=	GRCh38
NC_000001.10:g.169701072T= , CM000663.1:g.169701072T=	GRCh37
NC_000001.9:g.167967696T=	NCBI36
NG_012124.1:g.7149A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333360.12:c.433A= (SELE) MANE Select	ENSP00000331736.7:p.Asn145=
ENST00000333360.11:c.433A= (SELE)	ENSP00000331736.7:p.Asn145=
ENST00000367774.1:c.433A= (SELE)	ENSP00000356748.1:p.Asn145=
ENST00000367775.5:c.433A= (SELE)	ENSP00000356749.1:p.Asn145=
ENST00000367776.5:c.433A= (SELE)	ENSP00000356750.1:p.Asn145=
ENST00000367777.5:c.433A= (SELE)	ENSP00000356751.1:p.Asn145=
ENST00000461085.1:n.116A= (SELE)
ENST00000498289.5:n.851+47999T= (FIRRM)
NM_000450.2:c.433A= (SELE) MANE Select	NP_000441.2:p.Asn145=