Canonical Allele Identifier: CA1206206711

Gene: SELL FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169707431G= , CM000663.2:g.169707431G=	GRCh38
NC_000001.10:g.169676572G= , CM000663.1:g.169676572G=	GRCh37
NC_000001.9:g.167943196G=	NCBI36
NG_016132.1:g.9272C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236147.6:c.491C= (SELL) MANE Select	ENSP00000236147.5:p.Ser164=
ENST00000650983.1:c.530C= (SELL)	ENSP00000498227.1:p.Ser177=
ENST00000236147.4:c.530C= (SELL)	ENSP00000236147.4:p.Ser177=
ENST00000463108.5:n.691C= (SELL)
ENST00000466340.1:n.503C= (SELL)
ENST00000479657.5:n.243C= (SELL)
ENST00000498289.5:n.851+23499G= (FIRRM)
NM_000655.4:c.530C= (SELL)	NP_000646.2:p.Ser177=
NR_029467.1:n.459C= (SELL)
NM_000655.5:c.491C= (SELL) MANE Select	NP_000646.3:p.Ser164=
NR_029467.2:n.460C= (SELL)