Canonical Allele Identifier: CA1235753

Gene: SELL FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169704697G>A , CM000663.2:g.169704697G>A	GRCh38
NC_000001.10:g.169673838G>A , CM000663.1:g.169673838G>A	GRCh37
NC_000001.9:g.167940462G>A	NCBI36
NG_016132.1:g.12006C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000236147.6:c.637C>T (SELL) MANE Select	ENSP00000236147.5:p.Pro213Ser
ENST00000650983.1:c.676C>T (SELL)	ENSP00000498227.1:p.Pro226Ser
ENST00000236147.4:c.676C>T (SELL)	ENSP00000236147.4:p.Pro226Ser
ENST00000460650.5:n.57C>T (SELL)
ENST00000463108.5:n.837C>T (SELL)
ENST00000479657.5:n.389C>T (SELL)
ENST00000498289.5:n.851+20765G>A (FIRRM)
NM_000655.4:c.676C>T (SELL)	NP_000646.2:p.Pro226Ser
NR_029467.1:n.605C>T (SELL)
NM_000655.5:c.637C>T (SELL) MANE Select	NP_000646.3:p.Pro213Ser
NR_029467.2:n.606C>T (SELL)