Canonical Allele Identifier: CA1206206695

Gene: SELL FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169707410C= , CM000663.2:g.169707410C=	GRCh38
NC_000001.10:g.169676551C= , CM000663.1:g.169676551C=	GRCh37
NC_000001.9:g.167943175C=	NCBI36
NG_016132.1:g.9293G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236147.6:c.512G= (SELL) MANE Select	ENSP00000236147.5:p.Cys171=
ENST00000650983.1:c.551G= (SELL)	ENSP00000498227.1:p.Cys184=
ENST00000236147.4:c.551G= (SELL)	ENSP00000236147.4:p.Cys184=
ENST00000463108.5:n.712G= (SELL)
ENST00000466340.1:n.524G= (SELL)
ENST00000479657.5:n.264G= (SELL)
ENST00000498289.5:n.851+23478C= (FIRRM)
NM_000655.4:c.551G= (SELL)	NP_000646.2:p.Cys184=
NR_029467.1:n.480G= (SELL)
NM_000655.5:c.512G= (SELL) MANE Select	NP_000646.3:p.Cys171=
NR_029467.2:n.481G= (SELL)