Canonical Allele Identifier: CA2320796095

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184662_7184671delinsGGAAATAAAT , CM000681.2:g.7184662_7184671delinsGGAAATAAAT	GRCh38
NC_000019.9:g.7184673_7184682delinsGGAAATAAAT , CM000681.1:g.7184673_7184682delinsGGAAATAAAT	GRCh37
NC_000019.8:g.7135673_7135682delinsGGAAATAAAT	NCBI36
NG_008852.2:g.114330_114339delinsATTTATTTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-34_653-25delinsATTTATTTCC MANE Select	ENSP00000303830.4:n.653-34_653-25delinsATTTATTTCC
ENST00000302850.9:c.653-34_653-25delinsATTTATTTCC	ENSP00000303830.4:n.653-34_653-25delinsATTTATTTCC
ENST00000341500.9:c.653-34_653-25delinsATTTATTTCC	ENSP00000342838.4:n.653-34_653-25delinsATTTATTTCC
ENST00000598216.1:n.628-34_628-25delinsATTTATTTCC
NM_000208.2:c.653-34_653-25delinsATTTATTTCC	NP_000199.2:n.653-34_653-25delinsATTTATTTCC
NM_000208.3:c.653-34_653-25delinsATTTATTTCC	NP_000199.2:n.653-34_653-25delinsATTTATTTCC
NM_001079817.1:c.653-34_653-25delinsATTTATTTCC	NP_001073285.1:n.653-34_653-25delinsATTTATTTCC
NM_001079817.2:c.653-34_653-25delinsATTTATTTCC	NP_001073285.1:n.653-34_653-25delinsATTTATTTCC
XM_011527988.1:c.731-34_731-25delinsATTTATTTCC	XP_011526290.1:n.731-34_731-25delinsATTTATTTCC
XM_011527989.1:c.731-34_731-25delinsATTTATTTCC	XP_011526291.1:n.731-34_731-25delinsATTTATTTCC
XM_011527988.2:c.653-34_653-25delinsATTTATTTCC	XP_011526290.2:n.653-34_653-25delinsATTTATTTCC
XM_011527989.3:c.653-34_653-25delinsATTTATTTCC	XP_011526291.2:n.653-34_653-25delinsATTTATTTCC
NM_000208.4:c.653-34_653-25delinsATTTATTTCC MANE Select	NP_000199.2:n.653-34_653-25delinsATTTATTTCC
NM_001079817.3:c.653-34_653-25delinsATTTATTTCC	NP_001073285.1:n.653-34_653-25delinsATTTATTTCC