Canonical Allele Identifier: CA1206216879

Gene: SELE FIRRM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169731645_169731646delinsCA , CM000663.2:g.169731645_169731646delinsCA	GRCh38
NC_000001.10:g.169700786_169700787delinsCA , CM000663.1:g.169700786_169700787delinsCA	GRCh37
NC_000001.9:g.167967410_167967411delinsCA	NCBI36
NG_012124.1:g.7434_7435delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333360.12:c.529+189_529+190delinsTG (SELE) MANE Select	ENSP00000331736.7:n.529+189_529+190delinsTG
ENST00000333360.11:c.529+189_529+190delinsTG (SELE)	ENSP00000331736.7:n.529+189_529+190delinsTG
ENST00000367774.1:c.529+189_529+190delinsTG (SELE)	ENSP00000356748.1:n.529+189_529+190delinsTG
ENST00000367775.5:c.529+189_529+190delinsTG (SELE)	ENSP00000356749.1:n.529+189_529+190delinsTG
ENST00000367776.5:c.529+189_529+190delinsTG (SELE)	ENSP00000356750.1:n.529+189_529+190delinsTG
ENST00000367777.5:c.529+189_529+190delinsTG (SELE)	ENSP00000356751.1:n.529+189_529+190delinsTG
ENST00000461085.1:n.401_402delinsTG (SELE)
ENST00000498289.5:n.851+47713_851+47714delinsCA (FIRRM)
NM_000450.2:c.529+189_529+190delinsTG (SELE) MANE Select	NP_000441.2:n.529+189_529+190delinsTG