Canonical Allele Identifier: CA1206216990

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731928T= , CM000663.2:g.169731928T=	GRCh38
NC_000001.10:g.169701069T= , CM000663.1:g.169701069T=	GRCh37
NC_000001.9:g.167967693T=	NCBI36
NG_012124.1:g.7152A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333360.12:c.436A= (SELE) MANE Select	ENSP00000331736.7:p.Thr146=
ENST00000333360.11:c.436A= (SELE)	ENSP00000331736.7:p.Thr146=
ENST00000367774.1:c.436A= (SELE)	ENSP00000356748.1:p.Thr146=
ENST00000367775.5:c.436A= (SELE)	ENSP00000356749.1:p.Thr146=
ENST00000367776.5:c.436A= (SELE)	ENSP00000356750.1:p.Thr146=
ENST00000367777.5:c.436A= (SELE)	ENSP00000356751.1:p.Thr146=
ENST00000461085.1:n.119A= (SELE)
ENST00000498289.5:n.851+47996T= (FIRRM)
NM_000450.2:c.436A= (SELE) MANE Select	NP_000441.2:p.Thr146=