Canonical Allele Identifier: CA32482710

Gene: SELE FIRRM

Linked Data

• dbSNP Id: rs35940462
• MyVariant Identifiers: chr1:g.169700643_169700644insG (hg19) ; chr1:g.169731502_169731503insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731505dup , CM000663.2:g.169731505dup	GRCh38
NC_000001.10:g.169700646dup , CM000663.1:g.169700646dup	GRCh37
NC_000001.9:g.167967270dup	NCBI36
NG_012124.1:g.7577dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.529+332dup (SELE) MANE Select	ENSP00000331736.7:n.529+332dup
ENST00000333360.11:c.529+332dup (SELE)	ENSP00000331736.7:n.529+332dup
ENST00000367774.1:c.529+332dup (SELE)	ENSP00000356748.1:n.529+332dup
ENST00000367775.5:c.529+332dup (SELE)	ENSP00000356749.1:n.529+332dup
ENST00000367776.5:c.529+332dup (SELE)	ENSP00000356750.1:n.529+332dup
ENST00000367777.5:c.529+332dup (SELE)	ENSP00000356751.1:n.529+332dup
ENST00000461085.1:n.544dup (SELE)
ENST00000498289.5:n.851+47573dup (FIRRM)
NM_000450.2:c.529+332dup (SELE) MANE Select	NP_000441.2:n.529+332dup