Canonical Allele Identifier: CA2320806822

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7205096_7205097delinsAC , CM000681.2:g.7205096_7205097delinsAC	GRCh38
NC_000019.9:g.7205107_7205108delinsAC , CM000681.1:g.7205107_7205108delinsAC	GRCh37
NC_000019.8:g.7156107_7156108delinsAC	NCBI36
NG_008852.2:g.93904_93905delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-20460_653-20459delinsGT MANE Select	ENSP00000303830.4:n.653-20460_653-20459delinsGT
ENST00000302850.9:c.653-20460_653-20459delinsGT	ENSP00000303830.4:n.653-20460_653-20459delinsGT
ENST00000341500.9:c.653-20460_653-20459delinsGT	ENSP00000342838.4:n.653-20460_653-20459delinsGT
ENST00000598216.1:n.628-20460_628-20459delinsGT
NM_000208.2:c.653-20460_653-20459delinsGT	NP_000199.2:n.653-20460_653-20459delinsGT
NM_000208.3:c.653-20460_653-20459delinsGT	NP_000199.2:n.653-20460_653-20459delinsGT
NM_001079817.1:c.653-20460_653-20459delinsGT	NP_001073285.1:n.653-20460_653-20459delinsGT
NM_001079817.2:c.653-20460_653-20459delinsGT	NP_001073285.1:n.653-20460_653-20459delinsGT
XM_011527988.1:c.731-20460_731-20459delinsGT	XP_011526290.1:n.731-20460_731-20459delinsGT
XM_011527989.1:c.731-20460_731-20459delinsGT	XP_011526291.1:n.731-20460_731-20459delinsGT
XM_011527988.2:c.653-20460_653-20459delinsGT	XP_011526290.2:n.653-20460_653-20459delinsGT
XM_011527989.3:c.653-20460_653-20459delinsGT	XP_011526291.2:n.653-20460_653-20459delinsGT
NM_000208.4:c.653-20460_653-20459delinsGT MANE Select	NP_000199.2:n.653-20460_653-20459delinsGT
NM_001079817.3:c.653-20460_653-20459delinsGT	NP_001073285.1:n.653-20460_653-20459delinsGT